Inhibitors of mutant isocitrate dehydrogenases and compositions and methods thereof

ABSTRACT

The invention provides novel chemical compounds useful for treating cancer, or a related disease or disorder thereof, and pharmaceutical composition and methods of preparation and use thereof.

PRIORITY CLAIMS AND RELATED PATENT APPLICATIONS

This application claims the benefit of priority from U.S. Provisional Application Ser. No. 62/436,328, filed on Dec. 19, 2016, and 62/536,367, filed Jul. 24, 2017, the entire content of each of which is incorporated herein by reference in its entirety.

TECHNICAL FIELDS OF THE INVENTION

The invention generally relates to therapeutics and treatment methods for certain diseases and conditions. More particularly, the invention provides novel chemical compounds and pharmaceutical compositions thereof useful for treating cancer and methods of preparation and use thereof.

BACKGROUND OF THE INVENTION

Isocitrate dehydrogenase (IDH) is an enzyme that catalyzes the oxidative decarboxylation of isocitrate, producing alpha-ketoglutarate (α-ketoglutarate) and CO₂. IDH exists in three isoforms in humans: IDH3 catalyzes the third step of the citric acid cycle while converting NAD+ to NADH in the mitochondria. The isoforms IDH1 and IDH2 catalyze the same reaction outside the context of the citric acid cycle and use NADP+ as a cofactor instead of NAD+. IDHs localize to the cytosol as well as the mitochondrion and peroxisome.

Normal, wild type IDH enzymes help to break down nutrients and generate energy for cells. When mutated, IDH creates a molecule that alters the cells' genetic programming, and instead of maturing, the cells remain primitive and proliferate quickly. Non-mutant IDH 1/2 catalyzes the oxidative decarboxylation of isocitrate to α-ketoglutarate (α-KG) thereby reducing NAD+(NADP+) to NADP (NADPH), e.g., in the forward reaction.

IDH1 and IDH2 are mutated in a wide range of hematologic and solid tumor malignancies. Mutations of IDH 1/2 present in certain cancer cells result in a new ability of the enzyme to catalyze the NAPH-dependent reduction of -ketoglutarate to R (−)-2-hydroxyglutarate (2HG), which is not formed by wild-type IDH 1/2. Human IDH2 gene encodes a protein of 452 amino acids. (GenBank entries NM_002168.2 and NP 002159.2; The MGC Project Team 2004, Genome Res. 14:2121-2127). Human IDH1 gene encodes a protein of 414 amino acids (GenBank entries NM_005896.2 and NP 005887.2; Nekrutenko et al, 1998 Mol. Biol. Evol. 15:1674-1684; Geisbrecht et al, 1999 J. Biol. Chem. 274:30527-30533; Wiemann et al, 2001 Genome Res. 11:422-435; The MGC Project Team 2004 Genome Res. 14:2121-2127; Sjoeblom et al. 2006 Science 314:268-274.) 2HG production is believed to contribute to the formation and progression of cancer. (Dang, et al. 2009 Nature 462:739-44.)

There is an urgent and growing need for improved cancer therapeutics and treatment methods, e.g., via effective inhibition of mutant IDH 1/2 and their alpha hydroxyl neoactivity.

SUMMARY OF THE INVENTION

The invention provides novel, orally available, selective and potent inhibitors of mutated IDH 1 and/or IDH 2 proteins. The compounds disclosed here form irreversible covalent bond with mutant IDH 1 and/or IDH 2 protein and effectively inhibit their respective alpha hydroxyl activity.

In one aspect, the invention generally relates to a compound having the structure of formula (I)

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof.

In certain embodiments of, R_(E) comprises a group selected from:

In certain embodiments, the compound has the structural formula (II):

wherein,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ comprises a group selected from: piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl and azetidinyl moieties and/or comprises an electrophilic warhead selected from:

In certain embodiments of (I), having the structural formula (III)

wherein

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ comprises a group selected from: piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl and azetidinyl moiety and/or comprises of an electrophilic group selected from:

In another aspect, the invention generally relates to a pharmaceutical composition. The pharmaceutical composition includes a compound disclosed herein and a pharmaceutically acceptable excipient, carrier, or diluent.

In yet another aspect, the invention generally relates to a pharmaceutical composition comprising a compound having the structural formula of (I):

wherein,

each of R_(A) and R_(B) is independently H or a halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In certain embodiments of the pharmaceutical composition, R_(E) of the compound comprises a group selected from:

In yet another aspect, the invention generally relates to a pharmaceutical composition comprising a compound having the structural formula of (II):

wherein,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In yet another aspect, the invention generally relates to a pharmaceutical composition comprising a compound having the structural formula of (III):

wherein,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In yet another aspect, the invention generally relates to a unit dosage form comprising a pharmaceutical composition disclosed herein.

In yet another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula (I):

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof, or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula of (II):

wherein,

each of R_(A) and R_(B) is independently H or a halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula of (III):

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows exemplary Intact Mass spectrum of IDH1 R132C and labeled Mass Spectrum of IDH1 R132C treated with ISO1 and ISO3, respectively.

FIG. 2 shows exemplary Intact Mass of IDH1 R132C.

FIG. 3 shows exemplary Labeled Mass Spectrum of IDH1 R132C treated with ISO1.

DEFINITIONS

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. General principles of organic chemistry, as well as specific functional moieties and reactivity, are described in “Organic Chemistry”, Thomas Sorrell, University Science Books, Sausalito: 2006.

Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms. The present invention contemplates all such compounds, including cis- and trans-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention. Additional asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are intended to be included in this invention.

Isomeric mixtures containing any of a variety of isomer ratios may be utilized in accordance with the present invention. For example, where only two isomers are combined, mixtures containing 50:50, 60:40, 70:30, 80:20, 90:10, 95:5, 96:4, 97:3, 98:2, 99:1, or 100:0 isomer ratios are contemplated by the present invention. Those of ordinary skill in the art will readily appreciate that analogous ratios are contemplated for more complex isomer mixtures.

If, for instance, a particular enantiomer of a compound of the present invention is desired, it may be prepared by asymmetric synthesis, or by derivation with a chiral auxiliary, where the resulting diastereomeric mixture is separated and the auxiliary group cleaved to provide the pure desired enantiomers. Alternatively, where the molecule contains a basic functional group, such as amino, or an acidic functional group, such as carboxyl, diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional crystallization or chromatographic methods well known in the art, and subsequent recovery of the pure enantiomers.

As used herein, “administration” of a disclosed compound encompasses the delivery to a subject of a compound as described herein, or a prodrug or other pharmaceutically acceptable derivative thereof, using any suitable formulation or route of administration, as discussed herein.

As used herein, the term “electrophilic group” or “electrophile” refers to group or moiety that is attracted towards and capable of accepting a pair of electrons to form a new covalent bond. Exemplary electrophilic groups include an acrylamide group.

As used herein, the terms “effective amount” or “therapeutically effective amount” refer to that amount of a compound or pharmaceutical composition described herein that is sufficient to effect the intended application including, but not limited to, disease treatment, as illustrated below. In some embodiments, the amount is that effective for detectable killing or inhibition of the growth or spread of cancer cells; the size or number of tumors; or other measure of the level, stage, progression or severity of the cancer. The therapeutically effective amount can vary depending upon the intended application, or the subject and disease condition being treated, e.g., the desired biological endpoint, the pharmacokinetics of the compound, the disease being treated, the mode of administration, and the weight and age of the patient, which can readily be determined by one of ordinary skill in the art. The term also applies to a dose that will induce a particular response in target cells, e.g., reduction of cell migration. The specific dose will vary depending on, for example, the particular compounds chosen, the species of subject and their age/existing health conditions or risk for health conditions, the dosing regimen to be followed, the severity of the disease, whether it is administered in combination with other agents, timing of administration, the tissue to which it is administered, and the physical delivery system in which it is carried.

As used herein, the terms “treatment” or “treating” a disease or disorder refers to a method of reducing, delaying or ameliorating such a condition before or after it has occurred. Treatment may be directed at one or more effects or symptoms of a disease and/or the underlying pathology. Treatment is aimed to obtain beneficial or desired results including, but not limited to, therapeutic benefit and/or a prophylactic benefit. By therapeutic benefit is meant eradication or amelioration of the underlying disorder being treated. Also, a therapeutic benefit is achieved with the eradication or amelioration of one or more of the physiological symptoms associated with the underlying disorder such that an improvement is observed in the patient, notwithstanding that the patient can still be afflicted with the underlying disorder. For prophylactic benefit, the pharmaceutical compounds and/or compositions can be administered to a patient at risk of developing a particular disease, or to a patient reporting one or more of the physiological symptoms of a disease, even though a diagnosis of this disease may not have been made. The treatment can be any reduction and can be, but is not limited to, the complete ablation of the disease or the symptoms of the disease. As compared with an equivalent untreated control, such reduction or degree of prevention is at least 5%, 10%, 20%, 40%, 50%, 60%, 80%, 90%, 95%, or 100% as measured by any standard technique.

As used herein, the term “therapeutic effect” refers to a therapeutic benefit and/or a prophylactic benefit as described herein. A prophylactic effect includes delaying or eliminating the appearance of a disease or condition, delaying or eliminating the onset of symptoms of a disease or condition, slowing, halting, or reversing the progression of a disease or condition, or any combination thereof.

As used herein, the term “pharmaceutically acceptable ester” refers to esters that hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Such esters can act as a prodrug as defined herein. Pharmaceutically acceptable esters include, but are not limited to, alkyl, alkenyl, alkynyl, aryl, aralkyl, and cycloalkyl esters of acidic groups, including, but not limited to, carboxylic acids, phosphoric acids, phosphinic acids, sulfinic acids, sulfonic acids and boronic acids. Examples of esters include formates, acetates, propionates, butyrates, acrylates and ethylsuccinates. The esters can be formed with a hydroxy or carboxylic acid group of the parent compound.

As used herein, the term “pharmaceutically acceptable enol ethers” include, but are not limited to, derivatives of formula —C═C(OR) where R can be selected from alkyl, alkenyl, alkynyl, aryl, aralkyl and cycloalkyl. Pharmaceutically acceptable enol esters include, but are not limited to, derivatives of formula —C═C(OC(O)R) where R can be selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl and cycloalkyl.

As used herein, a “pharmaceutically acceptable form” of a disclosed compound includes, but is not limited to, pharmaceutically acceptable salts, esters, hydrates, solvates, isomers, prodrugs, and isotopically labeled derivatives of disclosed compounds. In one embodiment, a “pharmaceutically acceptable form” includes, but is not limited to, pharmaceutically acceptable salts, esters, isomers, prodrugs and isotopically labeled derivatives of disclosed compounds. In some embodiments, a “pharmaceutically acceptable form” includes, but is not limited to, pharmaceutically acceptable salts, esters, stereoisomers, prodrugs and isotopically labeled derivatives of disclosed compounds.

In certain embodiments, the pharmaceutically acceptable form is a pharmaceutically acceptable salt. As used herein, the term “pharmaceutically acceptable salt” refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of subjects without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, Berge et al. describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences (1977) 66:1-19. Pharmaceutically acceptable salts of the compounds provided herein include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchioric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, besylate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. In some embodiments, organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, lactic acid, trifluoracetic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, and the like.

The salts can be prepared in situ during the isolation and purification of the disclosed compounds, or separately, such as by reacting the free base or free acid of a parent compound with a suitable base or acid, respectively. Pharmaceutically acceptable salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N⁺(C₁₋₄ alkyl)⁴ salts. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, iron, zinc, copper, manganese, aluminum, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, lower alkyl sulfonate and aryl sulfonate. Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines, substituted amines, including naturally occurring substituted amines, cyclic amines, basic ion exchange resins, and the like, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, and ethanolamine. In some embodiments, the pharmaceutically acceptable base addition salt can be chosen from ammonium, potassium, sodium, calcium, and magnesium salts.

In certain embodiments, the pharmaceutically acceptable form is a “solvate” (e.g., a hydrate). As used herein, the term “solvate” refers to compounds that further include a stoichiometric or non-stoichiometric amount of solvent bound by non-covalent intermolecular forces. The solvate can be of a disclosed compound or a pharmaceutically acceptable salt thereof. Where the solvent is water, the solvate is a “hydrate”. Pharmaceutically acceptable solvates and hydrates are complexes that, for example, can include 1 to about 100, or 1 to about 10, or 1 to about 2, about 3 or about 4, solvent or water molecules. It will be understood that the term “compound” as used herein encompasses the compound and solvates of the compound, as well as mixtures thereof.

In certain embodiments, the pharmaceutically acceptable form is a prodrug. As used herein, the term “prodrug” (or “pro-drug”) refers to compounds that are transformed in vivo to yield a disclosed compound or a pharmaceutically acceptable form of the compound. A prodrug can be inactive when administered to a subject, but is converted in vivo to an active compound, for example, by hydrolysis (e.g., hydrolysis in blood). In certain cases, a prodrug has improved physical and/or delivery properties over the parent compound. Prodrugs can increase the bioavailability of the compound when administered to a subject (e.g., by permitting enhanced absorption into the blood following oral administration) or which enhance delivery to a biological compartment of interest (e.g., the brain or lymphatic system) relative to the parent compound. Exemplary prodrugs include derivatives of a disclosed compound with enhanced aqueous solubility or active transport through the gut membrane, relative to the parent compound.

The prodrug compound often offers advantages of solubility, tissue compatibility or delayed release in a mammalian organism (see, e.g., Bundgard, H., Design of Prodrugs (1985), pp. 7-9, 21-24 (Elsevier, Amsterdam). A discussion of prodrugs is provided in Higuchi, T., et al., “Pro-drugs as Novel Delivery Systems,” A.C.S. Symposium Series, Vol. 14, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated in full by reference herein. Exemplary advantages of a prodrug can include, but are not limited to, its physical properties, such as enhanced water solubility for parenteral administration at physiological pH compared to the parent compound, or it can enhance absorption from the digestive tract, or it can enhance drug stability for long-term storage.

As used herein, the term “pharmaceutically acceptable” excipient, carrier, or diluent refers to a pharmaceutically acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting the subject pharmaceutical agent from one organ, or portion of the body, to another organ, or portion of the body. Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not injurious to the patient. Some examples of materials which can serve as pharmaceutically-acceptable carriers include: sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients, such as cocoa butter and suppository waxes; oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol; polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate; agar; buffering agents, such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol; phosphate buffer solutions; and other non-toxic compatible substances employed in pharmaceutical formulations. Wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate, magnesium stearate, and polyethylene oxide-polypropylene oxide copolymer as well as coloring agents, release agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the compositions.

As used herein, the term “subject” refers to any animal (e.g., a mammal), including, but not limited to humans, non-human primates, rodents, and the like, which is to be the recipient of a particular treatment. Typically, the terms “subject” and “patient” are used interchangeably herein in reference to a human subject.

Compounds of the present invention are, subsequent to their preparation, preferably isolated and purified to obtain a composition containing an amount by weight equal to or greater than 95% (“substantially pure”), which is then used or formulated as described herein. In certain embodiments, the compounds of the present invention are more than 99% pure.

Solvates and polymorphs of the compounds of the invention are also contemplated herein. Solvates of the compounds of the present invention include, for example, hydrates.

Definitions of specific functional groups and chemical terms are described in more detail below. When a range of values is listed, it is intended to encompass each value and sub-range within the range. For example “C₁₋₆ alkyl” is intended to encompass, C₁, C₂, C₃, C₄, C₅, C₆, C₁₋₆, C₁₋₅, C₁₋₄, C₁₋₃, C₁₋₂, C₂₋₆, C₂₋₅, C₂₋₄, C₂₋₃, C₃₋₆, C₃₋₅, C₃₋₄, C₄₋₆, C₄₋₅, and C₅₋₆ alkyl.

As used herein, the term “alkyl” refers to a straight or branched hydrocarbon chain radical consisting solely of carbon and hydrogen atoms, containing no unsaturation, having from one to ten carbon atoms (e.g., C₁₋₁₀ alkyl). Whenever it appears herein, a numerical range such as “1 to 10” refers to each integer in the given range; e.g., “1 to 10 carbon atoms” means that the alkyl group can consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 10 carbon atoms, although the present definition also covers the occurrence of the term “alkyl” where no numerical range is designated. In some embodiments, “alkyl” can be a C₁₋₆ alkyl group. In some embodiments, alkyl groups have 1 to 10, 1 to 8, 1 to 6, or 1 to 3 carbon atoms. Representative saturated straight chain alkyls include, but are not limited to, -methyl, -ethyl, -n-propyl, -n-butyl, -n-pentyl, and -n-hexyl; while saturated branched alkyls include, but are not limited to, -isopropyl, -sec-butyl, -isobutyl, -tert-butyl, -isopentyl, 2-methylbutyl, 3-methylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2-methylhexyl, 3-methylhexyl, 4-methylhexyl, 5-methylhexyl, 2,3-dimethylbutyl, and the like. The alkyl is attached to the parent molecule by a single bond. Unless stated otherwise in the specification, an alkyl group is optionally substituted by one or more of substituents which independently include: acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylaryl, cycloalkyl, aralkyl, aryl, aryloxy, amino, amido, amidino, imino, azide, carbonate, carbamate, carbonyl, heteroalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxy, cyano, halo, haloalkoxy, haloalkyl, ester, ether, mercapto, thio, alkylthio, arylthio, thiocarbonyl, nitro, oxo, phosphate, phosphonate, phosphinate, silyl, sulfinyl, sulfonyl, sulfonamidyl, sulfoxyl, sulfonate, urea, —Si(R^(a))₃, —OR^(a), —SR^(a), —OC(O)—R^(a), —N(R^(a))₂, —C(O)R^(a), —C(O)OR^(a), —OC(O)N(R^(a))₂, —C(O)N(R^(a))₂, —N(R^(a))C(O)OR^(a), —N(R^(a))C(O)R^(a), —N(R^(a))C(O)N(R^(a))₂, —N(R^(a))C(NR^(a))N(R^(a))₂, —N(R^(a))S(O)_(t)N(R^(a))₂ (where t is 1 or 2), —P(═O)(R^(a))(R^(a)), or —O—P(═O)(OR^(a))₂ where each R^(a) is independently hydrogen, alkyl, haloalkyl, carbocyclyl, carbocyclylalkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl or heteroarylalkyl, and each of these moieties can be optionally substituted as defined herein. In a non-limiting embodiment, a substituted alkyl can be selected from fluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl, 3-fluoropropyl, hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, benzyl, and phenethyl.

As used herein, the term “alkoxy” refers to the group —O-alkyl, including from 1 to 10 carbon atoms (C₁₋₁₀) of a straight, branched, saturated cyclic configuration and combinations thereof, attached to the parent molecular structure through an oxygen. Examples include methoxy, ethoxy, propoxy, isopropoxy, butoxy, t-butoxy, pentoxy, cyclopropyloxy, cyclohexyloxy and the like. “Lower alkoxy” refers to alkoxy groups containing one to six carbons. In some embodiments, C₁₋₃ alkoxy is an alkoxy group which encompasses both straight and branched chain alkyls of from 1 to 3 carbon atoms. Unless stated otherwise in the specification, an alkoxy group can be optionally substituted by one or more substituents which independently include: acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylaryl, cycloalkyl, aralkyl, aryl, aryloxy, amino, amido, amidino, imino, azide, carbonate, carbamate, carbonyl, heteroalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxy, cyano, halo, haloalkoxy, haloalkyl, ester, ether, mercapto, thio, alkylthio, arylthio, thiocarbonyl, nitro, oxo, phosphate, phosphonate, phosphinate, silyl, sulfinyl, sulfonyl, sulfonamidyl, sulfoxyl, sulfonate, urea, —Si(R^(a))₃, —OR^(a), —SR^(a), —OC(O)—R^(a), —N(R^(a))₂, —C(O)R_(a), —C(O)OR^(a), —OC(O)N(R^(a))₂, —C(O)N(R^(a))₂, —N(R^(a))C(O)OR^(a), —N(R^(a))C(O)R^(a), —N(R^(a))C(O)N(R^(a))₂, —N(R^(a))C(NR^(a))N(R^(a))₂, —N(R^(a))S(O)_(t)N(R^(a))₂ (where t is 1 or 2), —P(═O)(R^(a))(R^(a)), or —O—P(═O)(OR^(a))₂ where each R^(a) is independently hydrogen, alkyl, haloalkyl, carbocyclyl, carbocyclylalkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl or heteroarylalkyl, and each of these moieties can be optionally substituted as defined herein.

As used herein, the terms “aromatic” or “aryl” refer to a radical with 6 to 14 ring atoms (e.g., C₆₋₁₄ aromatic or C₆₋₁₄ aryl) which has at least one ring having a conjugated pi electron system which is carbocyclic (e.g., phenyl, fluorenyl, and naphthyl). In some embodiments, the aryl is a C₆₋₁₀ aryl group. For example, bivalent radicals formed from substituted benzene derivatives and having the free valences at ring atoms are named as substituted phenylene radicals. In other embodiments, bivalent radicals derived from univalent polycyclic hydrocarbon radicals whose names end in“-yl” by removal of one hydrogen atom from the carbon atom with the free valence are named by adding “-idene” to the name of the corresponding univalent radical, e.g., a naphthyl group with two points of attachment is termed naphthylidene. Whenever it appears herein, a numerical range such as “6 to 14 aryl” refers to each integer in the given range; e.g., “6 to 14 ring atoms” means that the aryl group can consist of 6 ring atoms, 7 ring atoms, etc., up to and including 14 ring atoms. The term includes monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of ring atoms) groups. Polycyclic aryl groups include bicycles, tricycles, tetracycles, and the like. In a multi-ring group, only one ring is required to be aromatic, so groups such as indanyl are encompassed by the aryl definition. Non-limiting examples of aryl groups include phenyl, phenalenyl, naphthalenyl, tetrahydronaphthyl, phenanthrenyl, anthracenyl, fluorenyl, indolyl, indanyl, and the like. Unless stated otherwise in the specification, an aryl moiety can be optionally substituted by one or more substituents which independently include: acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylaryl, cycloalkyl, aralkyl, aryl, aryloxy, amino, amido, amidino, imino, azide, carbonate, carbamate, carbonyl, heteroalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxy, cyano, halo, haloalkoxy, haloalkyl, ester, ether, mercapto, thio, alkylthio, arylthio, thiocarbonyl, nitro, oxo, phosphate, phosphonate, phosphinate, silyl, sulfinyl, sulfonyl, sulfonamidyl, sulfoxyl, sulfonate, urea, —Si(R^(a))₃, —SR^(a), —OC(O)—R^(a), —N(R^(a))₂, —C(O)R_(a), —C(O)OR^(a), —OC(O)N(R^(a))₂, —C(O)N(R^(a))₂, —N(R^(a))C(O)OR^(a), —N(R^(a))C(O)R^(a), —N(R^(a))C(O)N(R^(a))₂, —N(R^(a))C(NR^(a))N(R^(a))₂, —N(R^(a))S(O)_(t)N(R^(a))₂ (where t is 1 or 2), —P(=O)(R^(a))(R^(a)), or —O—P(═O)(OR^(a))₂ where each R^(a) is independently hydrogen, alkyl, haloalkyl, carbocyclyl, carbocyclylalkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl or heteroarylalkyl, and each of these moieties can be optionally substituted as defined herein.

As used herein, the terms “cycloalkyl” and “carbocyclyl” each refers to a monocyclic or polycyclic radical that contains only carbon and hydrogen, and can be saturated or partially unsaturated. Partially unsaturated cycloalkyl groups can be termed “cycloalkenyl” if the carbocycle contains at least one double bond, or “cycloalkynyl” if the carbocycle contains at least one triple bond. Cycloalkyl groups include groups having from 3 to 13 ring atoms (i.e., C₃₋₁₃ cycloalkyl). Whenever it appears herein, a numerical range such as “3 to 10” refers to each integer in the given range; e.g., “3 to 13 carbon atoms” means that the cycloalkyl group can consist of 3 carbon atoms, 4 carbon atoms, 5 carbon atoms, etc., up to and including 13 carbon atoms. The term “cycloalkyl” also includes bridged and spiro-fused cyclic structures containing no heteroatoms. The term also includes monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of ring atoms) groups. Polycyclic aryl groups include bicycles, tricycles, tetracycles, and the like. In some embodiments, “cycloalkyl” can be a C₃₋₈ cycloalkyl radical. In some embodiments, “cycloalkyl” can be a C₃₋₅ cycloalkyl radical. Illustrative examples of cycloalkyl groups include, but are not limited to the following moieties: C₃₋₆ carbocyclyl groups include, without limitation, cyclopropyl (C₃), cyclobutyl (C₄), cyclopentyl (C₅), cyclopentenyl (C₅), cyclohexyl (C₆), cyclohexenyl (C₆), cyclohexadienyl (C₆) and the like. Examples of C₃₋₇ carbocyclyl groups include norbornyl (C₇). Examples of C₃₋₈ carbocyclyl groups include the aforementioned C₃₋₇ carbocyclyl groups as well as cycloheptyl (C₇), cycloheptadienyl (C₇), cycloheptatrienyl (C₇), cyclooctyl (C₈), bicyclo[2.2.1]heptanyl, bicyclo[2.2.2]octanyl, and the like. Examples of C₃₋₁₃ carbocyclyl groups include the aforementioned C₃₋₈ carbocyclyl groups as well as octahydro-1H indenyl, decahydronaphthalenyl, spiro[4.5]decanyl and the like. Unless stated otherwise in the specification, a cycloalkyl group can be optionally substituted by one or more substituents which independently include: acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylaryl, cycloalkyl, aralkyl, aryl, aryloxy, amino, amido, amidino, imino, azide, carbonate, carbamate, carbonyl, heteroalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxy, cyano, halo, haloalkoxy, haloalkyl, ester, ether, mercapto, thio, alkylthio, arylthio, thiocarbonyl, nitro, oxo, phosphate, phosphonate, phosphinate, silyl, sulfinyl, sulfonyl, sulfonamidyl, sulfoxyl, sulfonate, urea, —Si(R^(a))₃, —OR^(a), —SR^(a), —OC(O)—R^(a), —N(R^(a))₂, —C(O)R_(a), —C(O)OR^(a), —OC(O)N(R^(a))₂, —C(O)N(R^(a))₂, —N(R^(a))C(O)OR^(a), —N(R^(a))C(O)R^(a), —N(R^(a))C(O)N(R^(a))₂, —N(R^(a))C(NR^(a))N(R^(a))₂, —N(R^(a))S(O)_(t)N(R^(a))₂ (where t is 1 or 2), —P(═O)(R^(a))(R^(a)), or —O—P(═O)(OR^(a))₂ where each R^(a) is independently hydrogen, alkyl, haloalkyl, carbocyclyl, carbocyclylalkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl or heteroarylalkyl, and each of these moieties can be optionally substituted as defined herein. The terms “cycloalkenyl” and “cycloalkynyl” mirror the above description of “cycloalkyl” wherein the prefix “alk” is replaced with “alken” or “alkyn” respectively, and the parent “alkenyl” or “alkynyl” terms are as described herein. For example, a cycloalkenyl group can have 3 to 13 ring atoms, such as 5 to 8 ring atoms. In some embodiments, a cycloalkynyl group can have 5 to 13 ring atoms.

As used herein, the term “halide”, “halo”, or, alternatively, “halogen” means fluoro, chloro, bromo or iodo. The terms “haloalkyl,” “haloalkenyl,” “haloalkynyl” and “haloalkoxy” include alkyl, alkenyl, alkynyl and alkoxy structures that are substituted with one or more halo groups or with combinations thereof. For example, the terms “fluoroalkyl” and “fluoroalkoxy” include haloalkyl and haloalkoxy groups, respectively, in which the halo is fluorine, such as, but not limited to, trifluoromethyl, difluoromethyl, 2,2,2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl, and the like. Each of the alkyl, alkenyl, alkynyl and alkoxy groups are as defined herein and can be optionally further substituted as defined herein.

As used herein, the term “heteroalkyl” refers to an alkyl radical, which have one or more skeletal chain atoms selected from an atom other than carbon, e.g., oxygen, nitrogen, sulfur, phosphorus or combinations thereof. A numerical range can be given, e.g., C₁₋₄ heteroalkyl which refers to the chain length in total, which in this example is 4 atoms long. For example, a —CH₂OCH₂CH₃ radical is referred to as a “C₄” heteroalkyl, which includes the heteroatom center in the atom chain length description. Connection to the parent molecular structure can be through either a heteroatom or a carbon in the heteroalkyl chain. For example, an N-containing heteroalkyl moiety refers to a group in which at least one of the skeletal atoms is a nitrogen atom. One or more heteroatom(s) in the heteroalkyl radical can be optionally oxidized. One or more nitrogen atoms, if present, can also be optionally quaternized. For example, heteroalkyl also includes skeletal chains substituted with one or more nitrogen oxide (—O—) substituents. Exemplary heteroalkyl groups include, without limitation, ethers such as methoxyethanyl (—CH₂CH₂OCH₃), ethoxymethanyl (—CH₂OCH₂CH₃), (methoxymethoxy)ethanyl (—CH₂CH₂OCH₂OCH₃), (methoxymethoxy) methanyl (—CH₂OCH₂OCH₃) and (methoxyethoxy)methanyl (—CH₂OCH₂CH₂OCH₃) and the like; amines such as (—CH₂CH₂NHCH₃, —CH₂CH₂N(CH₃)₂, —CH₂NHCH₂CH₃, —CH₂N(CH₂CH₃)(CH₃)) and the like.

As used herein, the term “heteroaryl” or, alternatively, “heteroaromatic” refers to a refers to a radical of a 5-18 membered monocyclic or polycyclic (e.g., bicyclic, tricyclic, tetracyclic and the like) aromatic ring system (e.g., having 6, 10 or 14 π electrons shared in a cyclic array) having ring carbon atoms and 1-6 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, phosphorous and sulfur (“5-18 membered heteroaryl”). Heteroaryl polycyclic ring systems can include one or more heteroatoms in one or both rings. Whenever it appears herein, a numerical range such as “5 to 18” refers to each integer in the given range; e.g., “5 to 18 ring atoms” means that the heteroaryl group can consist of 5 ring atoms, 6 ring atoms, etc., up to and including 18 ring atoms. In some instances, a heteroaryl can have 5 to 14 ring atoms. In some embodiments, the heteroaryl has, for example, bivalent radicals derived from univalent heteroaryl radicals whose names end in “-yl” by removal of one hydrogen atom from the atom with the free valence are named by adding “-ene” to the name of the corresponding univalent radical, e.g., a pyridyl group with two points of attachment is a pyridylene.

For example, an N-containing “heteroaromatic” or “heteroaryl” moiety refers to an aromatic group in which at least one of the skeletal atoms of the ring is a nitrogen atom. One or more heteroatom(s) in the heteroaryl radical can be optionally oxidized. One or more nitrogen atoms, if present, can also be optionally quaternized. Heteroaryl also includes ring systems substituted with one or more nitrogen oxide (—O—) substituents, such as pyridinyl N-oxides. The heteroaryl is attached to the parent molecular structure through any atom of the ring(s).

“Heteroaryl” also includes ring systems wherein the heteroaryl ring, as defined above, is fused with one or more aryl groups wherein the point of attachment to the parent molecular structure is either on the aryl or on the heteroaryl ring, or wherein the heteroaryl ring, as defined above, is fused with one or more cycloalkyl or heterocycyl groups wherein the point of attachment to the parent molecular structure is on the heteroaryl ring. For polycyclic heteroaryl groups wherein one ring does not contain a heteroatom (e.g., indolyl, quinolinyl, carbazolyl and the like), the point of attachment to the parent molecular structure can be on either ring, i.e., either the ring bearing a heteroatom (e.g., 2-indolyl) or the ring that does not contain a heteroatom (e.g., 5-indolyl). In some embodiments, a heteroaryl group is a 5-10 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, phosphorous, and sulfur (“5-10 membered heteroaryl”). In some embodiments, a heteroaryl group is a 5-8 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, phosphorous, and sulfur (“5-8 membered heteroaryl”). In some embodiments, a heteroaryl group is a 5-6 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, phosphorous, and sulfur (“5-6 membered heteroaryl”). In some embodiments, the 5-6 membered heteroaryl has 1-3 ring heteroatoms selected from nitrogen, oxygen, phosphorous, and sulfur. In some embodiments, the 5-6 membered heteroaryl has 1-2 ring heteroatoms selected from nitrogen, oxygen, phosphorous, and sulfur. In some embodiments, the 5-6 membered heteroaryl has 1 ring heteroatom selected from nitrogen, oxygen, phosphorous, and sulfur.

Examples of heteroaryls include, but are not limited to, azepinyl, acridinyl, benzimidazolyl, benzindolyl, 1,3-benzodioxolyl, benzofuranyl, benzooxazolyl, benzo[d]thiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, benzo[b][1,4] oxazinyl, 1,4-benzodioxanyl, benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzoxazolyl, benzopyranyl, benzopyranonyl, benzofuranyl, benzopyranonyl, benzofurazanyl, benzothiazolyl, benzothienyl (benzothiophenyl), benzothieno[3,2-d]pyrimidinyl, benzotriazolyl, benzo[4,6]imidazo[1,2-a]pyridinyl, carbazolyl, cinnolinyl, cyclopenta[d]pyrimidinyl, 6,7-dihydro-5H-cyclopenta[4,5]thieno [2,3-d]pyrimidinyl, 5,6-dihydrobenzo[h]quinazolinyl, 5,6-dihydrobenzo[h]cinnolinyl, 6,7-dihydro-5H benzo[6,7]cyclohepta[1,2-c]pyridazinyl, dibenzofuranyl, dibenzothiophenyl, furanyl, furazanyl, furanonyl, furo [3,2-c]pyridinyl, 5,6,7,8,9,10-hexahydrocycloocta[d] pyrimidinyl, 5,6,7,8,9,10-hexahydrocycloocta[d]pyridazinyl, 5,6,7,8,9,10-hexahydrocycloocta[d]pyridinyl, isothiazolyl, imidazolyl, indazolyl, indolyl, indazolyl, isoindolyl, indolinyl, isoindolinyl, isoquinolyl, indolizinyl, isoxazolyl, 5,8-methano-5,6,7,8-tetrahydroquinazolinyl, naphthyridinyl, 1,6-naphthyridinonyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl, oxiranyl, 5,6,6a,7,8,9,10,10a-octahydrobenzo[h]quinazolinyl, 1-phenyl-1H-pyrrolyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyl, pyranyl, pyrrolyl, pyrazolyl, pyrazolo[3,4-d]pyrimidinyl, pyridinyl, pyrido[3,2-d]pyrimidinyl, pyrido[3,4-d]pyrimidinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, quinazolinyl, quinoxalinyl, quinolinyl, isoquinolinyl, tetrahydroquinolinyl, 5,6,7,8-tetrahydroquinazolinyl, 5,6,7,8-tetrahydrobenzo [4,5 ]thieno [2,3-d]pyrimdinyl, 6,7,8,9-tetrahydro-5H-cyclohepta[4,5]thieno [2,3-d]pyrimidinyl, 5,6,7,8-tetrahydropyrido[4,5-c]pyridazinyl, thiazolyl, thiadiazolyl, thiapyranyl, triazolyl, tetrazolyl, triazinyl, thieno[2,3-d]pyrimidinyl, thieno[3,2-d]pyrimidinyl, thieno [2,3-c]pridinyl, and thiophenyl (i.e., thienyl). Unless stated otherwise in the specification, a heteroaryl moiety can be optionally substituted by one or more substituents which independently include: acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylaryl, cycloalkyl, aralkyl, aryl, aryloxy, amino, amido, amidino, imino, azide, carbonate, carbamate, carbonyl, heteroalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxy, cyano, halo, haloalkoxy, haloalkyl, ester, ether, mercapto, thio, alkylthio, arylthio, thiocarbonyl, nitro, oxo, phosphate, phosphonate, phosphinate, silyl, sulfinyl, sulfonyl, sulfonamidyl, sulfoxyl, sulfonate, urea, —Si(R^(a))₃, —OR^(a), —SR^(a), —OC(O)—R^(a), —N(R^(a))₂, —C(O)R_(a), —C(O)OR^(a), —OC(O)N(R^(a))₂, —C(O)N(R^(a))₂, —N(R^(a))C(O)OR^(a), —N(R^(a))C(O)R^(a), —N(R^(a))C(O)N(R^(a))₂, —N(R^(a))C(NR^(a))N(R^(a))₂, —N(R^(a))S(O)_(t)N(R^(a))₂ (where t is 1 or 2), —P(═O)(R^(a))(R^(a)), or —O—P(═O)(OR^(a))₂ where each R^(a) is independently hydrogen, alkyl, haloalkyl, carbocyclyl, carbocyclylalkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl or heteroarylalkyl, and each of these moieties can be optionally substituted as defined herein.

DETAILED DESCRIPTION OF THE INVENTION

The invention is based on the unexpected discovery of novel, orally available, selective and potent inhibitors of mutated IDH 1 and/or IDH 2 proteins. The compounds disclosed here reversibly bind or form irreversible covalent bond with mutant IDH 1 and/or IDH 2 protein and effectively inhibit their respective alpha hydroxyl neoactivity.

Several IDH inhibitors are currently being studied including 556 (WO2013046136A1), GSK321 and AG-221. These compounds reportedly bind to IDH1, IDH2, or both IDH1 and IDH2 in a reversible manner.

The reported reversible inhibitors have shown less than optimal potency, selectivity and exposure time.

In contrast, the present invention provides a reversible or irreversible inhibition strategy that affords significant improved potency, selectivity and exposure time presumably due to the covalent bonding and a prolonged pharmacodynamics.

Among the novel compounds disclosed herein, some bear an electrophilic group that is suitable for reaction with IDH1, IDH2, or both IDH1 and IDH2 to form an irreversible covalent bond. For the reversible inhibitors of the invention, the compounds bind to IDH1, IDH2, or both IDH1 and IDH2 in a non-covalent manner.

Advantages of the approach disclosed herein include sustained target inhibition, which can be achieved with only transient exposure of the target to the inhibitor. This approach reduces the need to achieve pharmacological properties that would allow for sustained drug levels in vivo.

In one aspect, the invention generally relates to a compound having the structure of formula (I):

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof.

In certain embodiments of, R_(E) comprises a group selected from:

In certain embodiments of (I), the compound has the structural formula (II):

wherein,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ comprises a group selected from: piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl and azetidinyl moieties and/or comprises an electrophilic warhead selected from:

In certain embodiments, R₁ is H.

In certain embodiments, R₁ is a halogen atom.

In certain embodiments, R₂ is Q-R₆ wherein Q is CH₂, NH or O, R₆ comprises a group selected from:

In certain embodiments, R₂ is Q-R₆, wherein Q is CH₂, NH or O, and R₆ comprises a piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl or azetidinyl moiety and an electrophilic group.

In certain embodiments, R₆ is selected from the group consisting of:

In certain embodiments of (I), R_(A) is H, R_(B) is H, Z₁ is CH and Z₂ is CH, and the compound has the structural formula (II-1):

In certain embodiments, the compound is selected from the group consisting of:

In certain embodiments of (I), R_(A) is H, R_(B) is H, Z₁ is N and Z₂ is N, having the structural formula (II-2):

In certain embodiments, the compound is selected from the group consisting of:

In certain embodiments of (I), R_(A) is H, R_(B) is H, Z₁ is N and Z₂ is CH, and the compound has the structural formula (II-3):

In certain embodiments of (I), R_(A) and R_(B) together is —Y=CH—X—, wherein, X is S, O or NH and Y is CH or N, having the structural formula (II-4):

In certain embodiments, X is S and Y is CH.

In certain embodiments, X is O and Y is CH.

In certain embodiments, X is NH and Y is CH.

In certain embodiments, Z₁ and Z₂ is CH.

In certain embodiments, Z₁ is N and Z₂ is CH.

In certain embodiments, Z₁ is N and Z₂ is N.

In certain embodiments, the compound is selected from the group consisting of:

wherein R₃ comprises a cyclic saturated or unsaturated group with a 5- to 7-member ring selected from piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl and azetidinyl moieties consisting of an electrophilic group.

In certain embodiments, the compound is selected from the group consisting of:

In certain embodiments of (I), having the structural formula (III)

wherein

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ comprises a group selected from: piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl and azetidinyl moiety and/or comprises of an electrophilic group selected from:

In certain embodiments, R₁ is H.

In certain embodiments, R₁ is a halogen atom.

In certain embodiments, R₂ is Q-R₆, wherein Q is CH₂, NH or O, R₆ comprises a piperidinyl, piperazinyl, phenyl, pyridinyl, pyrrolyl or azetidinyl moiety and an electrophilic group selected from:

In certain embodiments, R₆ is selected from the group consisting of:

In certain embodiments of (III), R_(A) is H, R_(B) is H, Z₁ is N, Z₂ is CH, having structural formula (III-1):

In certain embodiments of (III), R_(A) is H, R_(B) is H, Z₁ is N, Z₂ is N, having structural formula (III-2):

In certain embodiments, exemplary compounds of (III-1) include:

In certain embodiments, exemplary compounds of (III-1) include:

In another aspect, the invention generally relates to a pharmaceutical composition. The pharmaceutical composition includes a compound disclosed herein and a pharmaceutically acceptable excipient, carrier, or diluent.

In another aspect, the invention generally relates to a pharmaceutical composition comprising a compound having the structural formula of (I):

wherein,

each of R_(A) and R_(B) is independently H or a halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In certain embodiments of the pharmaceutical composition, R_(E) of the compound comprises a group selected from:

In certain embodiments of the pharmaceutical composition, the compound has the structural formula of (II):

wherein, each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In certain embodiments of the pharmaceutical composition, the compound has the structural formula of (III):

wherein, each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively,

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In yet another aspect, the invention generally relates to a unit dosage form comprising a pharmaceutical composition disclosed herein.

In yet another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula (I):

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

R_(E) is a group comprising an electrophilic warhead,

or a pharmaceutically acceptable form thereof, or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula of (II):

wherein,

each of R_(A) and R_(B) is independently H or a halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In another aspect, the invention generally relates to a method for treating, reducing, or preventing a disease or disorder. The method includes: administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula of (III):

wherein,

each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively;

Z₁ and Z₂ is independently CH or N;

R₁ is H or a halogen atom; and

R₂ is a functional group that comprises an electrophilic group,

or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.

In certain embodiments of the methods, the one or more cancers comprise a blood cancer or a hematologic malignance.

In certain embodiments of the methods, the one or more cancers are selected from B-acute lymphoblastic leukemias, B-acute lymphoblastic leukemias, chronic myelomonocytic leukemia, cute myelogenous leukemia, lymphoma, myelodysplasia syndrome, myeloproliferative neoplasms and myeloproliferative neoplasms.

Any appropriate route of administration can be employed, for example, parenteral, intravenous, subcutaneous, intramuscular, intraventricular, intracorporeal, intraperitoneal, rectal, or oral administration. Most suitable means of administration for a particular patient will depend on the nature and severity of the disease or condition being treated or the nature of the therapy being used and on the nature of the active compound.

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the compounds described herein or derivatives thereof are admixed with at least one inert customary excipient (or carrier) such as sodium citrate or dicalcium phosphate or (i) fillers or extenders, as for example, starches, lactose, sucrose, glucose, mannitol, and silicic acid, (ii) binders, as for example, carboxymethylcellulose, alignates, gelatin, polyvinylpyrrolidone, sucrose, and acacia, (iii) humectants, as for example, glycerol, (iv) disintegrating agents, as for example, agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain complex silicates, and sodium carbonate, (v) solution retarders, as for example, paraffin, (vi) absorption accelerators, as for example, quaternary ammonium compounds, (vii) wetting agents, as for example, cetyl alcohol, and glycerol monostearate, (viii) adsorbents, as for example, kaolin and bentonite, and (ix) lubricants, as for example, talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, or mixtures thereof. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethyleneglycols, and the like. Solid dosage forms such as tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells, such as enteric coatings and others known in the art.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art, such as water or other solvents, solubilizing agents, and emulsifiers, such as for example, ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propyleneglycol, 1,3-butyleneglycol, dimethylformamide, oils, in particular, cottonseed oil, groundnut oil, corn germ oil, olive oil, castor oil, sesame oil, glycerol, tetrahydrofurfuryl alcohol, polyethyleneglycols, and fatty acid esters of sorbitan, or mixtures of these substances, and the like. Besides such inert diluents, the composition can also include additional agents, such as wetting, emulsifying, suspending, sweetening, flavoring, or perfuming agents.

Materials, compositions, and components disclosed herein can be used for, can be used in conjunction with, can be used in preparation for, or are products of the disclosed methods and compositions. It is understood that when combinations, subsets, interactions, groups, etc. of these materials are disclosed that while specific reference of each various individual and collective combinations and permutations of these compounds may not be explicitly disclosed, each is specifically contemplated and described herein. For example, if a method is disclosed and discussed and a number of modifications that can be made to a number of molecules including in the method are discussed, each and every combination and permutation of the method, and the modifications that are possible are specifically contemplated unless specifically indicated to the contrary. Likewise, any subset or combination of these is also specifically contemplated and disclosed. This concept applies to all aspects of this disclosure including, but not limited to, steps in methods using the disclosed compositions. Thus, if there are a variety of additional steps that can be performed, it is understood that each of these additional steps can be performed with any specific method steps or combination of method steps of the disclosed methods, and that each such combination or subset of combinations is specifically contemplated and should be considered disclosed.

Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms. The present invention contemplates all such compounds, including cis- and trans-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention. Additional asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are intended to be included in this invention.

Isomeric mixtures containing any of a variety of isomer ratios may be utilized in accordance with the present invention. For example, where only two isomers are combined, mixtures containing 50:50, 60:40, 70:30, 80:20, 90:10, 95:5, 96:4, 97:3, 98:2, 99:1, or 100:0 isomer ratios are contemplated by the present invention. Those of ordinary skill in the art will readily appreciate that analogous ratios are contemplated for more complex isomer mixtures.

If, for instance, a particular enantiomer of a compound of the present invention is desired, it may be prepared by asymmetric synthesis, or by derivation with a chiral auxiliary, where the resulting diastereomeric mixture is separated and the auxiliary group cleaved to provide the pure desired enantiomers. Alternatively, where the molecule contains a basic functional group, such as amino, or an acidic functional group, such as carboxyl, diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional crystallization or chromatographic methods well known in the art, and subsequent recovery of the pure enantiomers.

EXAMPLES The Synthesis of ISO1

Methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate(2) To a solution of methyl (S)-4-(1-aminoethyl)benzoate (1) (4.9 g, 22.7 mmol) in DCM (120 mL) was added di-tert-butyl dicarbonate (5.95 g, 27.3 mmol) and TEA (6.97 ml, 50 mmol). The solution was stirred for 7 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) as a white solid (6.2 g, 97.6%).

Tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate(3) To a cooled (0° C.) solution of methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) (7.89 g, 28.2 mmol) in THF (142 mL) was added a solution of LiAlH₄ (1.3 g, 33.84 mmol) in THF (17 mL) and the resulting mixture was stirred at room temperature for 30 min. The reaction mixture was quenched by addition of a 1N NaOH solution until gas evolution ceased. The reaction mixture was filtered, washed with EtOAc. After separation, the aqueous phase was washed with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) as a white solid (5.6 g, 79%). MS m/z178.08 [M−74+H]⁺.

Tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate(4) To a solution of tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) (2.5 g, 10 mmol) in DCM (50 mL) was added methanesulfonyl chloride (1.4 g, 12 mmol) and TEA (2.02 g, 20 mmol). The solution was stirred for 12 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) as a white solid (1.28 g, 47.4%). MS m/z196.1 [M−74+H]⁺.

Benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate(6) To a solution of tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) (1.28 g, 4.74 mmol) in DMF (6 mL) was added benzyl piperazine-1-carboxylate (1.15 g, 5.22 mmol) and K₂CO₃ (1.97 g, 14.22 mmol). The resulting mixture was heated at 80° C. for 3 h. Then it was extracted with EtOAc at room temperature and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) as a white solid (0.92 g, 42.8%). MS m/z454.26 [M+H]⁺.

Benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) To a solution of benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) (0.45 g, 1 mmol) in EtOAc, was added 4N HCl/EtOAc (8 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 3 h. A saturated sodium bicarbonate solution was added to the solution and the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) as a white solid (0.34 g, 97%). MS m/z354.21 [M+H]⁺.

(S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one(8) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichloropyrimidine (b) (6.1 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂ atmosphere. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added to the solution. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) as a white solid (4 g, 40.4%). MS m/z242.09 [M+H]⁺.

Benzyl 4-(4-4S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl) amino)ethyl)benzyl)piperazine-1-carboxylate (9) A solution of benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) (1.1 g, 3.11 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.83 g, 3.42 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc which was washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) as a white solid (0.67 g, 38.5%). MS m/z559.29[M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) A mixture of Benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) (0.67 g, 1.2 mmol) and 10% Pd—C (0.1 g) in ethanol (5 mL) is stirred under hydrogen for overnight. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as a white solid (0.42 g, 82%). MS m/z213.13/425.26[M+H]⁺.

(S)-3-(2-(((S)-1-(4-((4-acryloylpiperazin-1-yl)methyl)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO1) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.1 mg, 0.24 mmol) in dry acetonitrile (3 mL) was added DIEA (62 mg, 0.48 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (21.7 mg, 0.24 mmol) was added the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-acryloylpiperazin-1-yl)methyl)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO1) as a white solid (46 mg, 40%). MS m/z240.14/479.28[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 8.16 (d, J=5.1 Hz, 1H), 7.78 (s, 1H), 7.27 (d, J=7.2 Hz, 2H), 7.23-7.14 (m, 3H), 6.76 (dd, J=16.7, 10.5 Hz, 1H), 6.13-6.02 (m, 1H), 5.65 (dd, J=10.4, 2.4 Hz, 1H), 4.97 (s, 1H), 4.61 (s, 1H), 4.33 (dd, J=18.0, 9.7 Hz, 2H), 3.51 (s, 4H), 3.40 (d, J=29.6 Hz, 2H), 2.31 (s, 4H), 1.75 (s, 1H), 1.39 (t, J=17.0 Hz, 3H), 0.69 (dd, J=97.7, 44.6 Hz, 6H).

The Synthesis of ISO2

Methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) To a solution of methyl (S)-4-(1-aminoethyl)benzoate (1) (4.9 g, 22.7 mmol) in DCM (120 mL) was added di-tert-butyl dicarbonate (5.95 g, 27.3 mmol) and TEA (6.97 mL, 50 mmol). The solution was stirred for 7 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) as a white solid (6.2 g, 97.6%).

Tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) To a cooled (0° C.) solution of methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) (7.89 g, 28.2 mmol) in THF (142 mL) was added a solution of LiAlH₄ (1.3 g, 33.84 mmol) in THF (17 mL) and the resulting mixture was stirred at room temperature for 30 min. The reaction mixture was quenched by addition of a 1N NaOH solution until gas evolution ceased. The reaction mixture was filtered, washed with EtOAc. After separation, the aqueous phase was washed with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) as a white solid (5.6 g, 79%). MS m/z178 [M−74+H]⁺.

Tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) To a solution of tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) (2.5 g, 10 mmol) in DCM (50 mL) was added methanesulfonyl chloride (1.4 g, 12 mmol) and TEA (2.02 g, 20 mmol). The solution was stirred for 12 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) as a white solid (1.28 g, 47.4%). MS m/z196 [M−74+H]⁺.

Benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) To a solution of tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) (1.28 g, 4.74 mmol) in DMF (6 mL) was added benzyl piperazine-1-carboxylate (1.15 g, 5.22 mmol) and K₂CO₃ (1.97 g, 14.22 mmol). The resulting mixture was heated at 80° C. for 3 h. Then it was extracted with EtOAc and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) as a white solid (0.92 g, 42.8%). MS m/z454 [M+H]⁺.

Benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) To a solution of benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) (0.45 g, 1 mmol) in EtOAc (3 mL), was added 4N HCl/EtOAc (8 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 3 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) as a white solid (0.34 g, 97%). MS m/z354 [M+H]⁺.

(S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichloropyrimidine (b) (6.1 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂ atmosphere. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine and then was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) as a white solid (4 g, 40.4%). MS m/z242 [M+H]⁺.

Benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl) amino)ethyl)benzyl)piperazine-1-carboxylate (9) A solution of benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) (1.1 g, 3.11 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.83 g, 3.42 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) as a white solid (0.67 g, 38.5%). MS m/z559[M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) A mixture of Benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) (0.67 g, 1.2 mmol) and 10% Pd—C (0.1 g) in ethanol (5 mL) is stirred under hydrogen for overnight. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as a white solid (0.42 g, 82%). MS m/z213/425[M+H]⁺.

(S)-3-(2-(((S)-1-(4-((4-((E)-4-(dimethylamino)but-2-enoyl)piperazin-1-yl)methyl)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO2) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.21 g, 0.49 mmol) in dry acetonitrile (5 mL) was added DIEA (96 mg, 0.74 mmol). The resulting mixture was cooled down to −20° C. and then (E)-4-bromobut-2-enoyl chloride (0.13 g, 0.74 mmol) was added and the solution was stirred for 5 min. And then 2M dimethylamine solution in THF was added, and the resulting mixture was stirred at room temperature for 3 h. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-((E)-4-(dimethylamino)but-2-enoyl)piperazin-1-yl)methyl)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO2) as a white solid (50 mg, 15%). MS m/z536[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 8.20-8.10 (m, 1H), 7.80 (s, 1H), 7.35-7.25 (m, 2H), 7.25-7.15 (m, 3H), 6.85-6.77 (m, 1H), 6.66-6.56 (m, 1H), 4.97 (s, 1H), 4.61 (s, 1H), 4.41-4.22 (m, 2H), 3.66-3.43 (m, 8H), 2.59-2.51 (m, 4H), 2.41-2.24 (m, 4H), 1.74 (s, 1H), 1.41 (d, J=7.0 Hz, 3H), 0.78-0.35 (m, 6H).

The Synthesis of ISO3

(S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) To a solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (2 g, 10 mmol) in DCM (20 mL) was added di-tert-butyl dicarbonate (2.4 g, 11 mmol) and TEA (1.27 g, 12.4 mmol). The solution was stirred for 3 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) as a white solid (2.9 g, 96.7%).

Tert-butyl (S)-(1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)carbamate (4) The 5-nitropyridin-2-amine(3) (1.38 g, 9.9 mmol), CuI (0.86 g, 4.5 mmol) and anhydrous K₂CO₃ (2.49 g, 18 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen gas three times. A solution of (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) (2.69 g, 9 mmol) and DMEDA (0.4 g, 4.5 mmol) 1,4-dioxane (45 ml) was added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl was added the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided Tert-butyl (S)-(1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)carbamate (4) as a yellow solid (1.48 g, 46%).

(S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) To a solution of tert-butyl (S)-(1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)carbamate (4) (2.52 g, 7.03 mmol) in EtOAc (5 mL), was added 4N HCl/EtOAc (10 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 1.5 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) as a yellow solid (1.67 g, 92%).

(S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichloropyrimidine (b) (6.1 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) as a white solid (4 g, 40.4%). MS m/z242.09 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) A solution of (S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) (0.39 g, 1.5 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) (0.4 g, 1.65 mmol) in DMSO (3 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) as a solid (0.25 g, 36%). MS m/z217.61/464.2 [M+H]⁺.

(S)-3-(2-(((S)-1-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A mixture of (S)-4-isopropyl-3-(2-(((S)-1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) (0.25 g, 0.54 mmol) and 10% Pd—C (0.1 g) in MeOH (5 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.175 g, 75%). MS m/z217.61/434.22[M+H]⁺.

N-(6-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)pyridin-3-yl)acrylamide (ISO3) To a solution of (S)-3-(2-(((S)-1-(4-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (60 mg, 0.14 mmol) in dry acetonitrile (2 mL) was added DIEA (36 mg, 0.28 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (12.7 mg, 0.14 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (ISO3) as a solid (28 mg, 41%). MS m/z244.62/488.23[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 10.03 (s, 1H), 8.86 (s, 1H), 8.37 (d, J=2.5 Hz, 1H), 8.16 (d, J=5.6 Hz, 1H), 7.83 (dd, J=8.9, 2.6 Hz, 1H), 7.68 (s, 1H), 7.48 (t, J=11.9 Hz, 2H), 7.24-7.16 (m, 3H), 6.79 (d, J=8.9 Hz, 1H), 6.46-6.34 (m, 1H), 6.23 (dd, J=17.0, 2.0 Hz, 1H), 5.72 (dt, J=11.9, 5.9 Hz, 1H), 4.94 (s, 1H), 4.69-4.60 (m, 1H), 4.34 (dd, J=17.7, 9.1 Hz, 2H), 2.00 (dd, J=16.4, 7.2 Hz, 1H), 1.42 (d, J=7.0 Hz, 3H), 0.65 (d, J=91.7 Hz, 6H).

The Synthesis of ISO4

(S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) To a solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (2 g, 10 mmol) in DCM (20 mL) was added di-tert-butyl dicarbonate (2.4 g, 11 mmol) and TEA (1.27 g, 12.4 mmol). The solution was stirred for 3 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) as a white solid (2.9 g, 96.7%).

Tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate(4) The 4-nitroaniline (3) (1.01 g, 7.34 mmol), CuI (1.27 g, 6.67 mmol) and anhydrous K₂CO₃ (1.84 g. 13.34 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and back filled with nitrogen gas three times. A solution of (5)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) (2 g, 6.67 mmol) and DMEDA (0.59 g, 6.67 mmol) in 1,4-dioxane (30 mL) was added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided Tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate (4) as a yellow solid (1.2 g, 50.4%).

(S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) To a solution of tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate (4) (1.2 g, 3.36 mmol) in EtOAc (5 mL) was added 4N HCl/EtOAc (10 mL) in an ice bath. The resulting mixture was stirred at room temperature for 3 h and saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried, and concentrated. Silica gel column chromatography provided (S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) as a yellow solid (0.8 g, 93%).

(S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichloropyrimidine (b) (6.1 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂ atmosphere. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) as a white solid (4 g, 40.4%). MS m/z242.09 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) A solution of (S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) (0.24 g, 0.93 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) (0.25 g, 1.02 mmol) in DMSO (4 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) as a yellow solid (0.26 g, 60.5%). MS m/z463.205[M+H]⁺.

(S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A mixture of (S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (7) (0.16 g, 0.346 mmol) and 10% Pd—C(50 mg) in MeOH (2 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) as a solid (0.13 g, 86.7%). MS m/z433.23/217.12 [M+H]⁺.

N-(4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO4) To a solution of (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (80 mg, 0.185 mmol) in dry acetonitrile (3 mL) was added DIEA (48 mg, 0.37 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (16.7 mg, 0.185 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO4) as a solid (30 mg, 33.3%). MS m/z487.24[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 9.94 (s, 1H), 8.16 (d, J=5.6 Hz, 1H), 7.95 (s, 1H), 7.70 (s, 1H), 7.47 (dd, J=30.3, 8.6 Hz, 2H), 7.19 (t, J=6.9 Hz, 3H), 6.96 (dd, J=10.9, 8.7 Hz, 4H), 6.40 (dd, J=17.0, 10.1 Hz, 1H), 6.26-6.12 (m, 1H), 5.69 (dd, J=10.1, 2.1 Hz, 1H), 4.92 (s, 1H), 4.72-4.57 (m, 1H), 4.45-4.18 (m, 2H), 1.95 (d, J=31.0 Hz, 1H), 1.41 (d, J=7.0 Hz, 3H), 0.76 (s, 6H).

The Synthesis of ISO5

(S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichloropyrimidine (b) (6.1 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂ atmosphere. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) as a white solid (4 g, 40.4%). MS m/z242 [M+H]⁺.

(S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) A solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (4 g, 20 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) (5.3 g, 22 mmol) in DMSO (10 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) as a solid (4.2 g, 52%). MS m/z405 [M+H]⁺.

Tert-butyl (3-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)carbamate (5) The (S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) (1.01 g, 2.5 mmol), CuI (0.48 g, 2.5 mmol) and anhydrous K₂CO₃ (0.69 g. 2 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and back filled with nitrogen gas three times. A solution of tert-butyl (3-aminophenyl)carbamate (4) (1.04 g, 5 mmol) and DMEDA (0.22 g, 2.5 mmol) in 1,4-dioxane (12 mL) was added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. A saturated solution of NaCl was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (3-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)carbamate (5) (0.3 g, 23%). MS m/z533 [M+H]⁺.

(S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) To a solution of tert-butyl (3-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)carbamate (5) (0.3 g, 0.56 mmol) in EtOAc (1 mL), was added 4N HCl/EtOAc (2 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 1 h. The saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then the solution was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) as a solid (0.2 g, 83%). MS m/z433 [M+H]⁺.

N-(3-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO5) To a solution of (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) (0.1 g, 0.21 mmol) in dry acetonitrile (2 mL) was added DIEA (81.4 mg, 0.63 mmol). The resulting mixture was cooled to −20° C. and then acryloyl chloride (19.3 mg, 0.21 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(3-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO5) as a solid (35 mg, 34%). MS m/z487 [M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 9.96 (s, 1H), 8.16 (d, J=5.6 Hz, 1H), 8.08 (s, 1H), 7.70 (s, 1H), 7.50 (s, 1H), 7.29-7.15 (m, 3H), 7.15-7.08 (m, 1H), 7.07-6.94 (m, 2H), 6.69 (d, J=9.0 Hz, 1H), 6.41 (dd, J=17.0, 10.1 Hz, 1H), 6.22 (dd, J=17.0, 2.1 Hz, 1H), 5.80-5.61 (m, 1H), 4.94 (s, 1H), 4.71-4.52 (m, 1H), 4.35 (dd, J=16.8, 8.7 Hz, 2H), 2.10-1.82 (m, 1H), 1.42 (d, J=7.0 Hz, 3H), 1.28-1.21 (m, 1H), 0.92-0.69 (m, 3H), 0.68-0.42 (m, 3H).

The Synthesis of ISO6

5-bromo-2-(bromomethyl)pyrimidine (2) 5-bromo-2-methylpyrimidine (1) (1.73 g, 10 mmol) was dissolved in CCl₄ (17 mL) and treated with NBS (1.96 g, 11 mmol) and benzoylperoxide (0.48 g, 2 mmol). The reaction mixture was heated at 120° C. for 6 h. The reaction mixture was extracted with EtOAc and organic layers were washed with brine, dried over Na₂SO₄. Silica gel column chromatography provided 5-bromo-2-(bromomethyl)pyrimidine (2). MS m/z250 [M+H]⁺.

Benzyl 4-((5-bromopyrimidin-2-yl)methyl)piperazine-1-carboxylate (4) To a solution of benzyl piperazine-1-carboxylate (3) (0.85 g, 3.86 mmol) in dry DCM (10 mL) was added TEA (0.65 g, 6.44 mmol). The resulting mixture was cooled to 0° C., and then 5-bromo-2-(bromomethyl)pyrimidine (2) (0.81 g, 3.22 mmol) was added and the solution was stirred for 30 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided benzyl 4-((5-bromopyrimidin-2-yl)methyl)piperazine-1-carboxylate (4). MS m/z391 [M+H]+.

Benzyl 4-((5-acetylpyrimidin-2-yl)methyl)piperazine-1-carboxylate (6) PdCl₂(PPh₃)₂ (77 mg, 0.11 mmol) was added to a solution of benzyl 4-((5-bromopyrimidin-2-yl)methyl)piperazine-1-carboxylate (4) (0.86 g, 2.2 mmol) and tributyl(1-ethoxyvinyl)stannane (5) (0.87 g, 2.42 mmol) in THF (12 mL). The solution was degassed and filled with nitrogen and then was heated at 70° C. for 12 h. The reaction mixture was quenched with 2 M KF (10 mL) and extracted with EtOAc. The combined organic layers were washed with 2M KF, brine, dried over Na₂SO₄, and concentrated under vacuum to afford a yellow residue which was used in the next step without purification.

The above crude (2.2 mmol) was diluted with MeOH (6 mL) and 1M HCl (2 mL) added. The resulting yellow solution was stirred at room temperature for 2 h, and then the organic solvent was removed under reduced pressure. The residue was diluted with water, neutralized with 1N NaOH and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na₂SO₄. Silica gel column chromatography provided benzyl 4-((5-acetylpyrimidin-2-yl)methyl)piperazine-1-carboxylate (6). MS m/z355 [M+H]⁺.

Benzyl 4-((5-(1-aminoethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate(7) A 100 mL round-bottom flask was charged with a solution of benzyl 4-((5-acetylpyrimidin-2-yl)methyl)piperazine-1-carboxylate(6) (0.65 g, 1.83 mmol) in NH₃/EtOH (30 mL), acetic acid (1.1 g, 18.3 mmol) and NaBH₃CN (0.23 g, 3.66 mmol). The resulting solution was stirred at 90° C. for 3 h. The reaction progress was monitored by TLC. The pH was adjusted to 8 with NaOH/H₂O (3 mol/L). The resulting solution was extracted with DCM. Combined organic layers were dried over Na₂SO₄. Silica gel column chromatography provided benzyl 4-((5-(1-aminoethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate (7). MS m/z356 [M+H]+.

Benzyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate (9) A solution of benzyl 4-((5-(1-aminoethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate (7) (0.65 g, 1.83 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.53 g, 2.2 mmol) in DMSO (4 mL) was heated at 110° C. for 2 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided benzyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate (9) as a solid. MS m/z561[M+H]⁺.

(4S)-4-isopropyl-3-(2-((1-(2-(piperazin-1-ylmethyl)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) A mixture of benzyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)methyl)piperazine-1-carboxylate (9) (0.36 g, 0.64 mmol) and 10% Pd—C(50 mg) in ethanol (5 mL) is stirred under hydrogen for overnight. The mixture is filtered and concentrated. Silica gel column chromatography provided (4S)-4-isopropyl-3-(2-((1-(2-(piperazin-1-ylmethyl)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as a white solid (0.42 g, 82%). MS m/z427[M+H]⁺.

(4S)-3-(2-((1-(2-((4-acryloylpiperazin-1-yl)methyl)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO6) To a solution of (45)-4-isopropyl-3-(2-((1-(2-(piperazin-1-ylmethyl)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.12 g, 0.28 mmol) in dry acetonitrile (3 mL) was added DIEA (73 mg, 0.56 mmol). The resulting mixture was dropped to −20° C. and acryloyl chloride (31 mg, 0.34 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (4S)-3-(2-((1-(2-((4-acryloylpiperazin-1-yl)methyl)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one which was further purified by prep-TLC to obtain pure isomer as a white solid. (52 mg, 36%). MS m/z481 [M+H]+. ¹H NMR (400 MHz, DMSO) δ 8.74 (d, J=6.8 Hz, 2H), 8.19 (s, 1H), 7.94 (s, 1H), 7.28 (d, J=18.9 Hz, 1H), 6.88-6.65 (m, 1H), 6.09 (d, J=16.6 Hz, 1H), 5.66 (d, J=10.1 Hz, 1H), 4.99 (d, J=57.6 Hz, 1H), 4.73-4.54 (m, 1H), 4.42-4.17 (m, 2H), 3.82-3.62 (m, 2H), 3.61-3.42 (m, 4H), 1.76-1.58 (m, 1H), 1.54-1.43 (m, 3H), 1.29-1.22 (m, 2H), 0.91 (d, J=6.8 Hz, 2H), 0.84 (d, J=6.5 Hz, 3H), 0.76 (d, J=6.1 Hz, 3H).

The Synthesis of ISO7

6-chloronicotinoyl chloride (2) 6-chloronicotinic acid (1) (10 g, 63.5 mmol) was refluxed in thionylchloride (100 mL) under nitrogen for 3 h. volatiles were removed under reduced pressure.

1-(6-chloropyridin-3-yl)ethan-1-one (4) To a solution of 250 mL three-neck round-bottom flask with mechanical stirring containing magnesium chloride (1.7 g, 17.5 mmol) in dry toluene 25 mL was added triethylamine (6.1 g, 60 mmol) and by dimethyl malonate (3) (4 g, 30 mmol). The resulting mixture was stirred at 25° C. for 1.5 h and then 6-chioronicotinic acid chloride (2) (4.4 g, 25 mmol) was added in the solid form slowly in small portions over 45 min. Stirring was continued for 40 min before concentrated HCl (7.6 g, 77.5 mmol) was carefully added to quench the reaction. The toluene layer was separated and solvent was removed in vacuum to give a white needle-like solid. The solid was directly treated with DMSO (22 mL) and water (1 mL). The mixture was heated at 155° C. for 3 h and then it was cooled down to room temperature. It was then quenched with water, and the solid was collected by filtration. The solid was dissolved in DCM and dried over MgSO₄ and the solvent was removed under vacuum to give the product as a white solid.

Tert-butyl 4-((5-acetylpyridin-2-yl)oxy)piperidine-1-carboxylate (6) Tert-butyl 4-hydroxypiperidine-1-carboxylate (5) (1.4 g, 6.94 mmol) was added to a DMF suspension (10 mL) of 60% sodium hydride (0.25 g, 6.16 mmol) at 0° C. The solution was stirred at room temperature for 0.5 h. At 0° C., 1-(6-chloropyridin-3-yl)ethan-1-one (4) (0.9 g, 5.78 mmol) was added and the solution was stirred for 1 h. Water was added to the reaction solution, followed by extraction with EtOAc and subsequent sequential washing with water and saline and then the resulting organic layer was dried over Na₂SO₄. Silica gel column chromatography provided tert-butyl 4-((5-acetylpyridin-2-yl)oxy)piperidine-1-carboxylate (6) as a white solid. MS m/z321 [M+H]⁺.

Tert-butyl (S)-4-((5-(1-aminoethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate (7) A 100 mL round-bottom flask was charged with a solution of tert-butyl 4-((5-acetylpyridin-2-yl)oxy)piperidine-1-carboxylate (6) (0.26 g, 0.81 mmol) in NH₃/EtOH (13 mL), acetic acid (0.49 g, 8.1 mmol) and NaBH₃CN (0.1 g, 1.62 mmol). The resulting solution was stirred at 90° C. for 3 h. The reaction progress was monitored by TLC. The pH was adjusted to 8 with NaOH/H₂O (3 mol/L). The resulting solution was extracted with DCM. Combined organic layers were dried over Na₂SO₄. Silica gel column chromatography provided tert-butyl (S)-4-((5-(1-aminoethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate (7) as oil. MS m/z322 [M+H]+.

Tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate (9) A solution oft tert-butyl 44541-aminoethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate (7) (0.26 g, 0.81 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.22 g, 0.89 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate(9) as a solid. MS m/z527[M+H]⁺.

(S)-4-isopropyl-3-(2-((1-(6-(piperidin-4-yloxy)pyridin-3-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) To a solution of tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyridin-2-yl)oxy)piperidine-1-carboxylate (9) (0.2 g, 0.38 mmol) in EtOAc (2 mL), was added dropwise 4N HCl/EtOAc (6 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 3 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-((1-(6-(piperidin-4-yloxy)pyridin-3-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as solid. MS m/z427 [M+H]⁺.

(4S)-3-(2-((1-(6-((1-acryloylpiperidin-4-yl)oxy)pyridin-3-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO7) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(6-(piperidin-4-yloxy)pyridin-3-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.13 g, 0.3 mmol) in dry acetonitrile (2 mL) was added DIEA (78 mg, 0.36 mmol). The resulting mixture was cooled to −20° C. and then acryloyl chloride (33 mg, 0.36 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-3-(2-((1-(6-((1-acryloylpiperidin-4-yl)oxy)pyridin-3-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one. The pure diastereomer was obtained by prep-TLC. (52 mg, 36%). MS m/z481 [M+H]+. ¹H NMR (400 MHz, DMSO) δ 8.21-8.14 (m, 1H), 8.13-8.03 (m, 1H), 7.88-7.61 (m, 2H), 7.22 (dd, J=5.6, 3.9 Hz, 1H), 6.93-6.69 (m, 2H), 6.18-6.04 (m, 1H), 5.74-5.59 (m, 1H), 5.24-5.12 (m, 1H), 5.08-5.47 (m, 1H), 4.68-4.48 (m, 1H), 4.40-4.26 (m, 2H), 3.99-3.77 (m, 2H), 3.49-3.39 (m, 1H), 2.02-1.87 (m, 2H), 1.65-1.50 (m, 2H), 1.44 (d, J=6.9 Hz, 3H), 1.31-1.17 (m, 2H), 0.85 (dd, J=68.4, 6.8 Hz, 3H), 0.73-0.44 (m, 3H).

The Synthesis of ISO8

Tert-butyl (1-(4-nitrobenzyl)piperidin-4-yl)carbamate (3) To a solution of tert-butyl piperidin-4-ylcarbamate (1.0 g, 5.0 mmol) in dry dimethyl sulfoxide (30 mL) was added 1-(chloromethyl)-4-nitrobenzene (1.0 g, 5.8 mmol). The mixture was stirred at 90° C. The reaction mixture was quenched with water and extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.4 g, 40%). MS m/z 336 [M+H]+.

1-(4-nitrobenzyl)piperidin-4-amine (4) To a round-bottom flask containing tert-butyl (1-(4-nitrobenzyl)piperidin-4-yl)carbamate (0.25 g, 0.65 mmol) was added with hydrochloric acid (4N in ethyl acetate, 5 mL). The resulting solution was stirred at room temperature. The reaction mixture was quenched with saturated aqueous sodium bicarbonate and extracted with dichloromethane, concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.2 g, 95%).

(S)-4-isopropyl-3-(2-((1-(4-nitrobenzyl)piperidin-4-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (6) To a solution of 1-(4-nitrobenzyl)piperidin-4-amine (0.2 g, 0.85 mmol) in dry dimethyl sulfoxide (30 mL) was added (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (0.3 g, 1.2 mmol). The mixture was stirred at 90° C. The reaction mixture was quenched with water and extracted with dichloromethane. The combined extracts were dried and concentrated under reduced pressure. The residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.16 g, 50%). MS m/z 441 [M+H]+.

(S)-3-(2-((1-(4-aminobenzyl)piperidin-4-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) To a solution of (S)-4-isopropyl-3-(2-((1-(4-nitrobenzyl)piperidin-4-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (0.16 g, 0.25 mmol) in methanol (10 mL) was added Pd/C (0.2 g). The resulting mixture was stirred at room temperature under H₂. The organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (0.12 g, 95%). MS m/z411[M+H]+.

(S)—N-(4-((4-((4-(4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)piperidin-1-yl)methyl)phenyl)acrylamide (ISO8) To a solution of (S)-3-(2-((1-(4-aminobenzyl)piperidin-4-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) (0.12 g, 0.29 mmol) in dichloromethane (5 mL) was added triethylamine (60 mg, 0.45 mmol) and acryloyl chloride (28 mg, 0.33 mmol) at −30° C. The reaction mixture was diluted with water and saturated aqueous sodium bicarbonate. Dichloromethane was added and the organic layer was dried. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (25 mg, 20%). MS m/z 465[M+H]+. ¹H NMR (400 MHz, DMSO) δ 11.31 (s, 1H), 10.83 (s, 1H), 8.18 (d, J=5.4 Hz, 1H), 7.81 (d, J=8.4 Hz, 2H), 7.65-7.52 (m, 2H), 7.24 (d, J=5.2 Hz, 1H), 6.70-6.55 (m, 1H), 6.27 (dd, J=17.0, 1.9 Hz, 1H), 5.75 (dd, J=10.2, 1.9 Hz, 1H), 4.75-4.55 (m, 1H), 4.45-4.30 (m, 2H), 4.30-4.10 (m, 2H), 3.35-3.20 (m, 2H), 3.10-2.80 (m, 2H), 2.45-2.35 (m, 1H), 2.23-1.74 (m, 4H), 0.88 (d, J=9.4 Hz, 3H), 0.76 (d, J=6.8 Hz, 3H).

The Synthesis of ISO9

Tert-butyl (S)-(1-(4-nitrobenzyl)piperidin-3-yl)carbamate (3) To a solution of tert-butyl (S)-piperidin-3-ylcarbamate (1.0 g, 5.0 mmol) in dry dimethyl sulfoxide (30 mL) was added 1-(chloromethyl)-4-nitrobenzene (1.0 g, 5.8 mmol). The mixture was stirred for 1 h at 90° C. The reaction mixture was quenched with water and extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.4 g, 40%). MS m/z 336 [M+H]⁺.

(S)-1-(4-nitrobenzyl)piperidin-3-amine (4) To a round-bottom flask containing tert-butyl (S)-(1-(4-nitrobenzyl)piperidin-3-yl)carbamate (0.25 g, 0.65 mmol) was added with hydrochloric acid (4N in ethyl acetate, 5 mL). The resulting solution was stirred at room temperature. The reaction mixture was quenched with saturated aqueous sodium bicarbonate and extracted with dichloromethane, concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.2 g, 95%).

(S)-4-isopropyl-3-(2-(((S)-1-(4-nitrobenzyl)piperidin-3-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (6) To a solution of (S)-1-(4-nitrobenzyl)piperidin-3-amine (0.2 g, 0.85 mmol) in dry dimethyl sulfoxide (30 mL) was added (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (0.3 g, 1.2 mmol). The mixture was stirred at 90° C. The reaction mixture was quenched with water and extracted with dichloromethane. The combined extracts were dried and concentrated under reduced pressure. The residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.16 g, 50%). MS m/z 441 [M+H]⁺.

(S)-3-(2-(((S)-1-(4-aminobenzyl)piperidin-3-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(4-nitrobenzyl)piperidin-3-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (0.16 g, 0.25 mmol) in methanol (10 mL) was added Pd/C (0.2 g). The resulting mixture was stirred at room temperature under H₂. The organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (0.12 g, 95%). MS m/z 411[M+H]⁺.

N-(4-(((S)-3-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)piperidin-1-yl)methyl)phenyl)acrylamide (ISO9) To a solution of (S)-3-(2-(((S)-1-(4-aminobenzyl)piperidin-3-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) (0.12 g, 0.29 mmol) in dichloromethane (5 mL) was added triethylamine (60 mg, 0.45 mmol) and acryloyl chloride (28 mg, 0.33 mmol) at −30° C. The reaction mixture was diluted with water and saturated aqueous sodium bicarbonate. Dichloromethane was added and the organic layer was dried. Concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (25 mg, 20%). MS m/z 465[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 10.32 (s, 1H), 8.16 (d, J=5.5 Hz, 1H), 7.67 (s, 2H), 7.33 (s, 1H), 7.22 (s, 2H), 7.10-6.90 (m, 1H), 6.60-6.40 (m, 1H), 6.25 (dd, J=17.0, 1.6 Hz, 1H), 5.74 (d, J=10.1 Hz, 1H), 4.75-4.60 (m, 1H), 4.45-4.27 (m, 2H), 3.95-3.65 (m, 1H), 3.59-3.35 (m, 1H), 3.17 (d, J=4.9 Hz, 1H), 3.05-2.75 (m, 1H), 2.75-2.50 (m, 1H), 2.50-2.30 (m, 1H), 2.05-1.79 (m, 2H), 1.79-1.43 (m, 2H), 1.39-1.25 (m, 1H), 1.01-0.80 (m, 3H), 0.74 (d, J=6.9 Hz, 3H).

The Synthesis of ISO10

Tert-butyl (1-(4-nitrobenzyl)pyrrolidin-3-yl)carbamate (3) To a solution of tert-butyl pyrrolidin-3-ylcarbamate (1.0 g, 5.4 mmol) in dry dimethyl sulfoxide (30 mL) was added 1-(chloromethyl)-4-nitrobenzene (1.1 g, 6.1 mmol). The mixture was stirred for 1 h at 90° C. The reaction mixture was quenched with water and extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.3 g, 35%). MS m/z 322 [M+H]⁺.

1-(4-nitrobenzyl)pyrrolidin-3-amine (4) To a round-bottom flask containing tert-butyl (1-(4-nitrobenzyl)pyrrolidin-3-yl)carbamate (0.25 g, 0.65 mmol) was added with hydrochloric acid (4N in ethyl acetate, 5 mL). The resulting solution was stirred at room temperature. The reaction mixture was quenched with saturated aqueous sodium bicarbonate and extracted with dichloromethane, concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.2 g, 95%).

(4S)-4-isopropyl-3-(2-((1-(4-nitrobenzyl)pyrrolidin-3-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (6) To a solution of 1-(4-nitrobenzyl)pyrrolidin-3-amine (0.2 g, 0.85 mmol) in dry dimethyl sulfoxide (30 mL) was added (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (0.3 g, 1.2 mmol). The mixture was stirred at 90° C. The reaction mixture was then quenched with water and extracted with dichloromethane. The combined extracts were dried and concentrated under reduced pressure. The residue was purified by silica gel chromatography to afford the compound as a light yellow solid (0.12 g, 40%). MS m/z 427 [M+H]⁺.

(4S)-3-(2-((1-(4-aminobenzyl)pyrrolidin-3-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) To a solution of (4S)-4-isopropyl-3-(2-((1-(4-nitrobenzyl)pyrrolidin-3-yl)amino)pyrimidin-4-yl)oxazolidin-2-one (0.12 g, 0.20 mmol) in methanol (10 mL) was added Pd/C (0.2 g). The resulting mixture was stirred at room temperature under H₂. The organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (0.09 g, 95%). MS m/z 397[M+H]⁺.

N-(4-((3-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)pyrrolidin-1-yl)methyl)phenyl)acrylamide (ISO10) To a solution of (45)-3-(2-((1-(4-aminobenzyl)pyrrolidin-3-yl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (7) (0.09 g, 0.25 mmol) in dichloromethane (5 mL) was added triethylamine (48 mg, 0.36 mmol) and acryloyl chloride (21 mg, 0.28 mmol) at −30° C. The reaction mixture was diluted with water and saturated aqueous sodium bicarbonate. Dichloromethane was added and the organic layer was dried. Concentrated under reduced pressure and the residue was purified by silica gel chromatography to afford the compound as a white solid (22 mg, 31%). MS m/z 451[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ¹H NMR (400 MHz, DMSO) δ 11.60-11.22 (m, 1H), 10.58 (s, 1H), 8.21 (d, J=5.7 Hz, 1H), 7.83-7.65 (m, 2H), 7.51 (d, J=8.8 Hz, 2H), 7.32 (d, J=5.7 Hz, 1H), 6.55-6.42 (m, 1H), 6.29 (dd, J=17.0, 1.8 Hz, 1H), 5.80 (dd, J=10.1, 1.8 Hz, 1H), 4.78-4.60 (m, 2H), 4.55-4.25 (m, 4H), 3.58-3.40 (m, 2H), 3.25-2.93 (m, 2H), 2.20-2.01 (m, 2H), 0.95-0.75 (m, 3H), 0.74 (dd, J=16.9, 6.7 Hz, 3H).

The Synthesis of ISO11

Tert-butyl 4-((5-bromopyrimidin-2-yl)oxy)piperidine-1-carboxylate (3) Tert-butyl 4-hydroxypiperidine-1-carboxylate (2) (2.42 g, 12 mmol) was added to a DMF suspension (10 mL) of 60% sodium hydride (0.8 g, 20 mmol) at 0° C. and the solution was stirred at room temperature for 1 h. 5-bromo-2-chloropyrimidine (1) (1.93 g, 10 mmol) was then added and the solution was stirred for 1 h. Water was added to the reaction solution, followed by extraction with EtOAc and subsequent sequential washing with water and saline and then the resulting organic layer was dried over Na₂SO₄. Silica gel column chromatography provided tert-butyl 4-((5-bromopyrimidin-2-yl)oxy)piperidine-1-carboxylate (3) as a white solid. MS m/z358 [M+H]⁺.

1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethan-1-one (5) PdCl₂(PPh₃)₂ (0.21 g, 0.29 mmol) was added to a solution of tert-butyl 4-((5-bromopyrimidin-2-yl)oxy)piperidine-1-carboxylate (3) (2.11 g, 5.89 mmol) and tributyl(1-ethoxyvinyl)stannane (4) (2.34 g, 6.48 mmol) in THF (30 mL). The solution was degassed and filled with nitrogen twice and then it was heated at 70° C. for 12 h. The reaction mixture was quenched with 2 M KF (20 mL) and extracted with EtOAc. The combined organic layers were washed with 2M KF, brine, dried over Na₂SO₄, and concentrated under vacuum to afford a yellow residue which was used in the next step without purification.

The above crude (5.89 mmol) was diluted with MeOH (15 mL) and 1M HCl (5 mL) added. The resulting yellow solution was stirred at room temperature for 2 h, and then the organic solvent was removed under reduced pressure. The residue was diluted with water, the solution was neutralized with 1N NaOH and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na₂SO₄. Silica gel column chromatography provided 1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethan-1-one (5). MS m/z222 [M+H]⁺.

Tert-butyl 4-((5-acetylpyrimidin-2-yl)oxy)piperidine-1-carboxylate (6) To a solution of 1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethan-1-one (5) (0.22 g, 1 mmol) in DCM (5 mL) was added di-tert-butyl dicarbonate (0.26 g, 1.2 mmol) and TEA (0.2 g, 2 mmol). The solution was stirred for 2 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl 4-((5-acetylpyrimidin-2-yl)oxy)piperidine-1-carboxylate (6). MS m/z322 [M+H]⁺.

Tert-butyl 4-((5-(1-aminoethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate(7) A 100 mL round-bottom flask was charged with a solution of tert-butyl 4-((5-acetylpyrimidin-2-yl)oxy)piperidine-1-carboxylate (6) (1 g, 3.11 mmol) in NH₃/EtOH (50 mL), acetic acid (1.87 g, 31.1 mmol) and NaBH₃CN (0.39 g, 6.22 mmol). The resulting solution was stirred at 90° C. for 3 h. The reaction progress was monitored by TLC. The pH was adjusted to 8 with NaOH/H₂O (3 mol/L). The resulting solution was extracted with DCM. Combined organic layers were dried over Na₂SO₄. Silica gel column chromatography provided tert-butyl 4-((5-(1-aminoethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (7). MS m/z323 [M+H]+.

Tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (9) A solution of tert-butyl 44541-aminoethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (7) (0.95 g, 3 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.8 g, 3.3 mmol) in DMSO (10 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (9) as a solid. MS m/z528[M+H]⁺.

(4S)-4-isopropyl-3-(2-((1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) To a solution of tert-butyl 4-((5-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (9) (0.4 g, 0.76 mmol) in EtOAc (2 mL), was added 4N HCl/EtOAc (6 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 1 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (4S)-4-isopropyl-3-(2-((1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as solid. MS m/z428 [M+H]⁺.

(4S)-3-(2-((1-(2-((1-acryloylpiperidin-4-yl)oxy)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO11) To a solution of (45)-4-isopropyl-3-(2-((1-(2-(piperidin-4-yloxy)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.15 g, 0.35 mmol) in dry acetonitrile (2 mL) was added DIEA (90 mg, 0.7 mmol). The resulting mixture was cooled to −20° C. and then acryloyl chloride (38 mg, 0.42 mmol) was added, the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (4S)-3-(2-((1-(2-((l-acryloylpiperidin-4-yl)oxy)pyrimidin-5-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one as a white solid (52 mg, 36%). pure diastereomer was obtained by prep-TLC. MS m/z482 [M+H]+. ¹H NMR (400 MHz, DMSO) δ 8.65-8.50 (m, 2H), 8.18 (d, J=5.7 Hz, 1H), 7.81 (s, 1H), 7.25 (dd, J=5.7, 3.3 Hz, 1H), 6.88-6.78 (m, 1H), 6.15-6.02 (m, 1H), 5.67 (dd, J=10.5, 2.4 Hz, 1H), 5.20-5.10 (m, 1H), 5.05-4.95 (m, 1H), 4.66-4.57 (m, 1H), 4.45-4.25 (m, 2H), 3.95-3.75 (m, 2H), 3.50-3.40 (m, 1H), 2.05-1.90 (m, 2H), 1.68-1.58 (m, 2H), 1.48 (d, J=7.0 Hz, 3H), 1.35-1.15 (m, 2H), 0.97-0.72 (m, 3H), 0.56 (s, 3H).

The Synthesis of ISO12

1-(5-bromopyrimidin-2-yl)ethan-1-ol (2) 5-bromo-2-iodopyrimidine (1) (10 g, 35.1 mmol) was dissolved in THF (150 mL) and methylmagnesium chloride (3 M in Et₂O, 24 mL) was added at −78° C., then the mixture was stirred at −78° C. for 1 h. Acetaldehyde (4.64 g, 105.3 mmol) was added dropwise to the solution and the reaction was allowed to stir whilst warming to 0° C. over 1 h. MeOH was then added and the mixture concentrated under reduced pressure. The resultant solid was dissolved in DCM and washed with brine. Silica gel column chromatography provided 1-(5-bromopyrimidin-2-yl)ethan-1-ol (2). MS m/z204 [M+H]⁺.

2-(1-azidoethyl)-5-bromopyrimidine (3) A round-bottom flask containing 1-(5-bromopyrimidin-2-yl)ethan-1-ol (2) (2.92 g, 14.4 mmol) was charged with TEA (1.75 g, 17.3 mmol) and anhydrous DCM (30 mL) at ambient temperature. The resulting mixture was allowed to stir at room temperature for 3 h and the volatile components were removed under reduced pressure. The residue was dissolved in DMF (45 mL) and treated with NaN₃ (1.87 g, 28.8 mmol). The resulting mixture was stirred at room temperature for 24 h and was then partitioned between EtOAc and brine. Combined organic layer were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided 2-(1-azidoethyl)-5-bromopyrimidine (3).

1-(5-bromopyrimidin-2-yl)ethan-1-amine (4) A mixture of 2-(1-azidoethyl)-5-bromopyrimidine (3) (1.37 g, 6 mmol) and PPh₃ (2.04 g, 9 mmol) in MeOH (10 mL). was heated at 80° C. for 3 h. Then it was extracted with EtOAc and organic layers were washed with water and brine, dried (Na₂SO₄). The mixture is filtered and concentrated. Silica gel column chromatography provided 1-(5-bromopyrimidin-2-yl)ethan-1-amine (4). MS m/z203[M+H]⁺.

Tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5) To a solution of 1-(5-bromopyrimidin-2-yl)ethan-1-amine (4) (1.1 g, 5.4 mmol) in DCM (15 mL) was added di-tert-butyl dicarbonate (1.3 g, 5.94 mmol) and TEA (1.1 g, 10.8 mmol). The solution was stirred for 4 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5).

Tert-butyl (1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)carbamate (7) The N-methyl-4-nitroaniline (6) (0.85 g, 3.1 mmol), X-Phos (0.14 g), Pd₂(dba)₃ (55 mg) and anhydrous K₂CO₃ (0.77 g, 5.6 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen. A solution of tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5) (0.85 g, 2.8 mmol) in toluene (12 ml), were added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)carbamate (7). MS m/z374[M+H]⁺.

2-(1-aminoethyl)-N-methyl-N-(4-nitrophenyl)pyrimidin-5-amine (8) To a solution of tert-butyl (1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)carbamate (7) (0.45 g, 1.2 mmol) in EtOAc (2 mL) was added 4N HCl/EtOAc (8 mL) in an ice bath. The resulting mixture was stirred at room temperature for 1.5 h and saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided 2-(1-aminoethyl)-N-methyl-N-(4-nitrophenyl)pyrimidin-5-amine (8).

(4S)-4-isopropyl-3-(2-((1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) A solution of 2-(1-aminoethyl)-N-methyl-N-(4-nitrophenyl)pyrimidin-5-amine (8) (0.25 g, 0.9 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (9) (0.22 g, 0.9 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (4S)-4-isopropyl-3-(2-((1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as a solid. MS m/z479 [M+H]⁺.

(4S)-3-(2-((1-(5-((4-aminophenyl)(methyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11) A mixture of (4S)-4-isopropyl-3-(2-((1-(5-(methyl(4-nitrophenyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.2 g, 0.4 mmol) and 10% Pd—C(0.1 g) in MeOH (5 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (45)-3-(2-((1-(5-((4-aminophenyl) (methyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11). MS m/z449 [M+H]⁺.

N-(4-((2-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-5-yl)(methyl)amino)phenyl)acrylamide (ISO12) To a solution of (4S)-3-(2-((1-(5-((4-aminophenyl)(methyl)amino)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11) (0.12 g, 0.27 mmol) in dry acetonitrile (2 mL) was added DIEA (70 mg, 0.54 mmol). The resulting mixture was cooled down to −20° C., and then was added with acryloyl chloride (24 mg, 0.27 mmol). The solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(4-((2-(1-((4-4S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-5-yl)(methyl)amino)phenyl)acrylamide as a solid (30 mg, 22%). Pure diastereomer was obtained by prep-TLC. MS m/z503[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 10.32 (s, 1H), 8.29 (d, J=5.1 Hz, 2H), 8.19-8.11 (m, 1H), 7.71 (d, J=8.5 Hz, 2H), 7.56-7.31 (m, 1H), 7.21 (d, J=5.4 Hz, 1H), 7.18-7.05 (m, 2H), 6.56-6.42 (m, 1H), 6.29-6.20 (m, 1H), 5.74 (dd, J=10.1, 1.6 Hz, 1H), 5.01-4.89 (m, 1H), 4.70-4.17 (m, 3H), 3.27 (d, J=4.3 Hz, 3H), 2.58-2.51 (m, 1H), 1.47 (t, J=7.2 Hz, 3H), 0.96-0.72 (m, 3H), 0.71-0.48 (m, 3H).

The Synthesis of ISO13

1-(5-bromopyrimidin-2-yl)ethan-1-ol (2) 5-bromo-2-iodopyrimidine (1) (10 g, 35.1 mmol) was dissolved in THF (150 mL) and methyl magnesium chloride (3 M in Et₂O, 24 mL) was added at −78° C., then the mixture was stirred at −78° C. for 1 h. Acetaldehyde (4.64 g, 105.3 mmol) was added dropwise to the resulting solution and the reaction was allowed to stir whilst warming to 0° C. over 1 h. MeOH was added and the mixture concentrated in vacuo. The resultant solid was dissolved in DCM and washed with brine. Silica gel column chromatography provided 1-(5-bromopyrimidin-2-yl)ethan-1-ol (2). MS m/z204 [M+H]⁺.

2-(1-azidoethyl)-5-bromopyrimidine (3) A round-bottom flask containing 1-(5-bromopyrimidin-2-yl)ethan-1-ol (2) (2.92 g, 14.4 mmol) was charged with TEA (1.75 g, 17.3 mmol) and DCM (30 mL) at room temperature. The resulting mixture was allowed to stir at room temperature for 3 h and the volatile components were removed under reduced pressure. The residue was dissolved in DMF (45 mL) and treated with NaN₃ (1.87 g, 28.8 mmol). The resulting mixture was stirred at room temperature for 24 h and was then partitioned between EtOAc and brine. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided 2-(1-azidoethyl)-5-bromopyrimidine (3).

1-(5-bromopyrimidin-2-yl)ethan-1-amine (4) A mixture of 2-(1-azidoethyl)-5-bromopyrimidine (3) (1.37 g, 6 mmol) and PPh₃ (2.04 g, 9 mmol) in MeOH (10 mL). The resulting mixture was heated at 80° C. for 3 h. Then it was extracted with EtOAc and organic layers were washed with water and brine, dried (Na₂SO₄). The mixture is filtered and concentrated. Silica gel column chromatography provided 1-(5-bromopyrimidin-2-yl)ethan-1-amine (4). MS m/z203[M+H]⁺.

Tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5) To a solution of 1-(5-bromopyrimidin-2-yl)ethan-1-amine (4) (1.1 g, 5.4 mmol) in DCM (15 mL) was added di-tert-butyl dicarbonate (1.3 g, 5.94 mmol) and TEA (1.1 g, 10.8 mmol). The solution was stirred for 4 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5).

Tert-butyl (1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)carbamate(7) The (3-nitrophenyl)boronic acid (6) (0.62 g, 3.72 mmol), Pd(PPh₃)₄ (0.1 g) and anhydrous K₂CO₃ (0.69 g, 4.96 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen. A solution of tert-butyl (1-(5-bromopyrimidin-2-yl)ethyl)carbamate (5) (0.75 g, 2.48 mmol) in THF (12 mL) and H₂O (5 mL) was added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled down to room temperature. Then a saturated solution of NaCl was added and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)carbamate (7). MS m/z345[M+H]⁺.

1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethan-1-amine (8) To a solution of tert-butyl (1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)carbamate (7) (0.55 g, 1.6 mmol) in EtOAc (2 mL) was added 4N HCl/EtOAc (10 mL) in an ice bath. The resulting mixture was stirred at room temperature for 1.5 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided 1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethan-1-amine (8).

(4S)-4-isopropyl-3-(2-((1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) A solution of 1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethan-1-amine (8) (0.4 g, 1.6 mmol) and (S)-3-(2-chloropyrimidin-4-yl)-4-isopropyloxazolidin-2-one (9) (0.46 g, 1.92 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (4S)-4-isopropyl-3-(2-((1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) as a solid. MS m/z450 [M+H]⁺.

(4S)-3-(2-((1-(5-(3-aminophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11) A mixture of (45)-4-isopropyl-3-(2-((1-(5-(3-nitrophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)oxazolidin-2-one (10) (0.3 g, 0.67 mmol) and 10% Pd—C(0.1 g) in MeOH (5 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (4S)-3-(2-((1-(5-(3-aminophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11). MS m/z420 [M+H]⁺.

N-(3-(2-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-5-yl)phenyl)acrylamide (ISO13) To a solution of (4S)-3-(2-((1-(5-(3-aminophenyl)pyrimidin-2-yl)ethyl)amino)pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (11) (0.12 g, 0.29 mmol) in dry acetonitrile (2 mL) was added DIEA (75 mg, 0.58 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (31 mg, 0.34 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(3-(2-(1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)pyrimidin-2-yl)amino)ethyl)pyrimidin-5-yl)phenyl)acrylamide (ISO13) as a solid (30 mg, 22%). Pure diastereomer was obtained by prep-TLC. MS m/z474[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 10.46 (d, J=4.0 Hz, 1H), 9.00 (s, 1H), 8.88 (s, 1H), 8.24-8.10 (m, 1H), 8.05 (s, 1H), 7.80-7.72 (m, 1H), 7.71-7.61 (m, 1H), 7.51-7.39 (m, 2H), 7.25-7.18 (m, 1H), 6.57-6.45 (m, 1H), 6.34-6.28 (m, 1H), 5.82-5.74 (m, 1H), 5.20-4.91 (m, 1H), 4.55-4.11 (m, 3H), 2.62-2.53 (m, 1H), 1.62-1.50 (m, 3H), 0.99-0.72 (m, 3H), 0.61-0.31 (m, 3H).

Reaction Scheme for the Synthesis of ISO14

Methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) To a solution of methyl (S)-4-(1-aminoethyl)benzoate (1) (4.9 g, 22.7 mmol) in dichloromethane (120 mL) was added di-tert-butyl dicarbonate (5.95 g, 27.3 mmol) and TEA (6.97 ml, 50 mmol). The solution was stirred for 7 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography (EtOAc/PE 0 to 30%) provided methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) as a white solid (6.2 g, 97.6%).

Tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) To a cooled (0° C.) solution of methyl (S)-4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate (2) (7.89 g, 28.2 mmol) in THF (142 mL) was added a solution of LiAlH₄ (1.3 g, 33.84 mmol) in THF (17 mL) and the resulting mixture was stirred at room temperature for 30 min. The reaction mixture was quenched by addition of a 1N NaOH solution until gas evolution ceased. The reaction mixture was filtered, washed with EtOAc. After separation, the aqueous phase was extracted with EtOAc. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography (EtOAc/PE 0 to 30%) provided tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) as a white solid (5.6 g, 79%). MS m/z178.08 [M−74+H]⁺.

Tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) To a solution of tert-butyl (S)-(1-(4-(hydroxymethyl)phenyl)ethyl)carbamate (3) (2.5 g, 10 mmol) in dichloromethane (50 mL) was added methanesulfonyl chloride (1.4 g, 12 mmol) and TEA (2.02 g, 20 mmol). The solution was stirred for 12 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography (EtOAc/PE 0 to 20%) provided tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) as a white solid (1.28 g, 47.4%). MS m/z196.1 [M−74+H]⁺.

Benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) To a solution of tert-butyl (S)-(1-(4-(chloromethyl)phenyl)ethyl)carbamate (4) (1.28 g, 4.74 mmol) in DMF (6 mL) was added benzyl piperazine-1-carboxylate(1.15 g, 5.22 mmol) and K₂CO₃ (1.97 g, 14.22 mmol). The resulting mixture was heated at 80° C. for 3 h. Then it was extracted with EtOAc and organic layers were washed with water and brine, dried, and concentrated. Silica gel column chromatography provided benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) as a white solid (0.92 g, 42.8%). MS m/z454.26 [M+H]⁺.

Benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) To a solution of benzyl (S)-4-(4-(1-((tert-butoxycarbonyl)amino)ethyl)benzyl)piperazine-1-carboxylate (6) (0.45 g, 1 mmol) in EtOAc (3 mL), was added 4N HCl/EtOAc (8 mL) in an ice bath. The resulting mixture was stirred at room temperature for 3 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then the solution was extracted with EtOAc. Organic layers were dried, and concentrated. Silica gel column chromatography (EtOAc/PE 0 to 50%) provided benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) as a white solid (0.34 g, 97%). MS m/z354.21 [M+H]⁺.

(S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A solution of (S)-4-isopropyloxazolidin-2-one (A) (1.3 g, 10 mmol) and 2,4-dichlorothieno[3,2-d]pyrimidine (B) (2 g, 10 mmol) in 10 mL DMF was cooled to 0° C. under N₂. NaH (0.52 g of 60% suspension, 13 mmol) was slowly added to the solution and the temperature was kept below 5° C. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 3 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organics were dried, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) as a white solid. MS m/z298.1 [M+H]⁺.

Benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) A solution of benzyl (S)-4-(4-(1-aminoethyl)benzyl)piperazine-1-carboxylate (7) (0.35 g, 1 mmol) and (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.3 g, 1 mmol) in DMSO (5 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)benzyl)piperazine-1-carboxylate (9) as a white solid. MS m/z615.21 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)thieno [3,2-]pyrimidin-4-yl)oxazolidin-2-one (10) A mixture of benzyl 4-(4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl) benzyl)piperazine-1-carboxylate (9) (0.61 g, 1 mmol) and 10% Pd—C(0.61 g) in ethanol (5 mL) is stirred under hydrogen for overnight. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (10). MS m/z481.23 [M+H]+.

(S)-3-(2-(((S)-1-(4-((4-acryloylpiperazin-1-yl)methyl)phenyl)ethyl)amino)thieno [3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO14) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperazin-1-ylmethyl)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (10) (39 mg, 0.081 mmol) in dry acetonitrile (1 mL) was added DIEA (21 mg, 0.162 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (15 mg, 0.612 mmol) was added and resulting solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried, and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-acryloylpiperazin-1-yl)methyl)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO14) as a white solid. MS m/z535.21 [M+H]⁺. 1H NMR (400 MHz, DMSO-d₆) δ 8.15 (d, J=5.6 Hz, 1H), 7.71 (br, 1H), 7.33 (d, J=7.7 Hz, 2H), 7.21 (d, J=7.7 Hz, 2H), 7.10 (d, J=5.6 Hz, 1H), 6.76 (m, 10.4, 4.2 Hz, 1H), 6.08 (m, 2.7 Hz, 1H), 5.65 (m, 1H), 5.08 (s, 1H), 4.80 (s, 1H), 4.52 (m, 1H), 4.33 (m, 1H), 3.46-3.56 (m, 4H), 3.42 (s, 2H), 3.41-3.37 (m, 1H), 2.30 (s, 4H), 1.44 (d, J=7.0 Hz, 3H), 0.48 (m, 6H).

Reaction Scheme for the Synthesis of ISO17

(S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) To a solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (2 g, 10 mmol) in DCM (20 mL) was added di-tert-butyl dicarbonate (2.4 g, 11 mmol) and TEA (1.27 g, 12.4 mmol). The solution was stirred for 3 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) as a white solid (2.9 g, 96.7%).

Tert-butyl (S)-(1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)carbamate (4) The 5-nitropyridin-2-amine (3) (1.38 g, 9.9 mmol), CuI (0.95 g, 5 mmol) and K₂CO₃ (2.49 g. 18 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen gas three times. A solution of (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) (2.69 g, 9 mmol) and DMEDA (0.44 g, 5 mmol) in dioxane (45 mL), were added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)carbamate (4) as a yellow solid.

(S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) To a solution of Tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate (4) (1.2 g, 3.35 mmol) in EtOAc, was added 4N HCl/EtOAc (10 mL) in an ice bath. The resulting mixture was stirred at room temperature for 3 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) as a yellow solid.

(S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichlorothieno[3,2-d]pyrimidine (b) (8.4 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) as a white solid. MS m/z298 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (7) A solution of (S)—N-(4-(1-aminoethyl)phenyl)-5-nitropyridin-2-amine (5) (0.46 g, 1.55 mmol) and (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) (0.4 g, 1.55 mmol) in DMSO (10 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (7) as a yellow solid. MS m/z520[M+H]⁺.

(S)-3-(2-(((S)-1-(4-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A mixture of (S)-4-isopropyl-3-(2-(((S)-1-(4-((5-nitropyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (7) (0.27 g, 0.52 mmol) and 10% Pd—C(0.1 g) in MeOH (5 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8). MS m/z490 [M+H]⁺.

N-(6-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)pyridin-3-yl)acrylamide (ISO17) To a solution of (S)-3-(2-(((S)-1-(4-((5-aminopyridin-2-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (0.14 g, 0.286 mmol) in dry acetonitrile (3 mL) was added DIEA (74 mg, 0.572 mmol). The resulting mixture was cooled down to −20° C., and then adding acryloyl chloride (26 mg, 0.286 mmol), stirring for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(6-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)pyridin-3-yl)acrylamide (ISO17) as a solid (54 mg, 35%). MS m/z544[M+H]⁺. ¹H NMR (400 MHz, DMSO) δ 10.03 (s, 1H), 8.86 (s, 1H), 8.36 (d, J=2.5 Hz, 1H), 8.13 (d, J=5.5 Hz, 1H), 7.82 (dd, J=8.9, 2.6 Hz, 1H), 7.70-7.53 (m, 1H), 7.53-7.44 (m, 2H), 7.30-7.20 (m, 2H), 7.10 (d, J=5.6 Hz, 1H), 6.78 (d, J=8.9 Hz, 1H), 6.45-6.35 (m, 1H), 6.26-6.17 (m, 1H), 5.79-5.65 (m, 1H), 5.15-4.75 (m, 2H), 4.53 (t, J=8.9 Hz, 1H), 4.40-4.27 (m, 1H), 2.57-2.51 (m, 1H), 1.45 (d, J=7.0 Hz, 3H), 0.87-0.42 (m, 6H).

Reaction Scheme for the Synthesis of ISO18

(S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) To a solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (2 g, 10 mmol) in DCM (20 mL) was added di-tert-butyl dicarbonate (2.4 g, 11 mmol) and TEA (1.27 g, 12.4 mmol). The solution was stirred for 3 h at room temperature then washed with water and brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) as a white solid (2.9 g, 96.7%).

Tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate (4) The 4-nitroaniline (3) (1.01 g, 7.34 mmol), CuI (1.27 g, 6.67 mmol) and anhydrous K₂CO₃ (1.84 g. 13.34 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen. A solution of (S)-2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)ethan-1-ylium (2) (2 g, 6.67 mmol) and DMEDA (0.59 g, 6.67 mmol) in 1,4-dioxane (30 mL) were added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl were added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate(4) as a yellow solid.

(S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) To a solution of tert-butyl (S)-(1-(4-((4-nitrophenyl)amino)phenyl)ethyl)carbamate (4) (1.2 g, 3.36 mmol) in EtOAc, was added 4N HCl/EtOAc (10 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 3 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc and organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) as a yellow solid.

(S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichlorothieno[3,2-d]pyrimidine (b) (8.4 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂ atmosphere. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) as a white solid. MS m/z298 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)thieno[3,2-41] pyrimidin-4-yl)oxazolidin-2-one (7) A solution of (S)-4-(1-aminoethyl)-N-(4-nitrophenyl)aniline (5) (0.4 g, 1.55 mmol) and (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (6) (0.46 g, 1.55 mmol) in DMSO (10 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (7) as a yellow solid. MS m/z519[M+H]⁺.

(S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) A mixture of (S)-4-isopropyl-3-(2-(((S)-1-(4-((4-nitrophenyl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (7) (0.26 g, 0.5 mmol) and 10% Pd—C(0.1 g) in MeOH (5 mL) is stirred under hydrogen for 2 h. The mixture is filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8). MS m/z489 [M+H]⁺.

N-(4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO18) To a solution of (S)-3-(2-(((S)-1-(4-((4-aminophenyl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (8) (70 mg, 0.14 mmol) in dry acetonitrile (1 mL) was added DIEA (36 mg, 0.28 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (13 mg, 0.14 mmol) was added and the resulted solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided N-(4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)phenyl)acrylamide (ISO18) as a solid (30 mg, 39%). MS m/z543[M+H]⁺.

Reaction Scheme for the Synthesis of ISO19

(S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) A solution of (S)-4-isopropyloxazolidin-2-one (a) (5.3 g, 41 mmol) and 2,4-dichlorothieno[3,2-d]pyrimidine (b) (8.4 g, 41 mmol) in 30 mL DMF was cooled to 0° C. under N₂. NaH (2.1 g of 60% suspension, 53 mmol) was slowly added. After 5 min, cold bath was removed. Reaction mixture was allowed to warm to room temperature and stirred 12 h. The reaction mixture was diluted with water and extracted with EtOAc. Organic layer was washed water, and brine. Combined organic layers were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) as a white solid. MS m/z298 [M+H]⁺.

(S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) A solution of (S)-1-(4-bromophenyl)ethan-1-amine (1) (4 g, 20 mmol) and (S)-3-(2-chlorothieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (2) (6.5 g, 22 mmol) in DMSO (10 mL) was heated at 110° C. for 3 h. The reaction mixture was extracted with EtOAc and organic layers were washed with water. After separation, the aqueous phase was extracted with EtOAc. Combined organics were dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) as a solid. MS m/z462 [M+H]⁺.

Tert-butyl 4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)piperidine-1-carboxylate (5) The tert-butyl 4-aminopiperidine-1-carboxylate (4) (0.23 g, 1.14 mmol), X-Phos (30 mg), Pd₂(dba)₃ (15 mg) and anhydrous K₂CO₃ (0.26 g, 1.9 mmol) were added to a Schlenk-type, three-neck flask fitted with a thermometer, magnetic stirrer bar and septum. The flask was evacuated and filled with nitrogen. A solution of (S)-3-(2-(((S)-1-(4-bromophenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (3) (0.44 g, 0.95 mmol) in 1,4-dioxane (12 mL), was added by syringe at room temperature. The reaction mixture was stirred at 100° C. for 12 h and then cooled to room temperature. And a saturated solution of NaCl was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered and concentrated. Silica gel column chromatography provided tert-butyl 4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)piperidine-1-carboxylate (5). MS m/z581 [M+H]⁺.

(S)-4-isopropyl-3-(2-(((S)-1-(4-(piperidin-4-ylamino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (6) To a solution of tert-butyl 4-((4-((S)-1-((4-((S)-4-isopropyl-2-oxooxazolidin-3-yl)thieno[3,2-d]pyrimidin-2-yl)amino)ethyl)phenyl)amino)piperidine-1-carboxylate (5) (0.29 g, 0.5 mmol) in EtOAc (2 mL), was added 4N HCl/EtOAc (8 mL) in an ice bath. And the resulting mixture was stirred at room temperature for 1 h. And saturated sodium bicarbonate solution was added dropwise, the pH was adjusted to 8-9, then was extracted with EtOAc. The organic layers were dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperidin-4-ylamino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (6) as a solid. MS m/z481 [M+H]⁺.

(S)-3-(2-(((S)-1-(4-((1-acryloylpiperidin-4-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO19) To a solution of (S)-4-isopropyl-3-(2-(((S)-1-(4-(piperidin-4-ylamino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)oxazolidin-2-one (6) (0.1 g, 0.21 mmol) in dry acetonitrile (2 mL) was added DIEA (81.4 mg, 0.63 mmol). The resulting mixture was cooled down to −20° C., and then acryloyl chloride (19.3 mg, 0.21 mmol) was added and the solution was stirred for 5 min. Then it was extracted with DCM and organic layers were washed with water and brine, dried (Na₂SO₄), and concentrated. Silica gel column chromatography provided (S)-3-(2-(((S)-1-(4-((1-acryloylpiperidin-4-yl)amino)phenyl)ethyl)amino)thieno[3,2-d]pyrimidin-4-yl)-4-isopropyloxazolidin-2-one (ISO19) as a solid. MS m/z535 [M+H]⁺.

TABLE 1 IC50 (M) of Exemplary Compounds Compound ID: IDH1 (R132H) IDH1 (R132C) IDH1 IS01 1.32E-09 1.61E-09 9.46E-06 IS03 3.61E-09 3.35E-09 8.52E-06 IS04 1.05E-08 7.55E-09 >1.00E-05 IS05 4.67E-09 >1.48E-06 IS07 3.40E-07 NA NA IS012 1.61E-07 1.98E-07 NA IS013 1.07E-07 2.85E-07 NA IS014 8.09E-1O 2.61 E-09 NA

Experimental Testing for Biological Activities

Compounds were tested against 3 enzymes WT IDH1, IDH1 R132C, IDH1 R132H

Assay Format: The production or depletion of NADPH by IDH enzymes was measured by diaphorase/resazurin coupled detection.

Assay Protocol on IDH1 Reaction Procedure Wild-Type:

1. Deliver enzyme/NADP in the reaction buffer into wells of reaction plate except No Enzyme control wells. Add buffer+NADP into No Enzyme wells. 2. Deliver compound in 100% DMSO into the enzyme mixture. Spin down and preincubate for 60 min at room temperature. 3. Deliver Substrate mixture to initiate the reaction. Spin down plate and gently shake 45 minutes at room temperature.

Detection Step for Wt:

4. Make a 3× mix of Detection mixture in the reaction buffer, and add detection mixture into the reaction. Spin down. 5. Incubate at room temperature for 10 minutes.

6. Measure in Envision. (Ex/Em=535/590 nm)

7. Subtract background (the average value of the No Enzyme control wells) from raw data. Average the DMSO control wells and set value as 100%. Take ratio of measured data/average DMSO control value times 100% to arrive at % activity.

Reaction Procedure Mutant:

8. Deliver enzyme/NADPH in the reaction buffer into wells of reaction plate except No Enzyme control wells. Add buffer+NADPH into No Enzyme wells. 9. Deliver compound in 100% DMSO into the enzyme mixture. Spin down and preincubate for 60 min at room temperature. 10. Deliver Substrate mixture to initiate the reaction. Spin down plate and gently shake 45 minutes at room temperature.

Detection Step (the Same as Wt):

11. Make a 3× mix of Detection mixture in the reaction buffer, and add detection mixture into the reaction. Spin down. 12. Incubate at room temperature for 10 minutes.

13. Measure in Envision. (Ex/Em=535/590 nm)

14. Subtract raw data from background (the average value of the No Enzyme wells). Average the DMSO control wells and set value as 100%. Take ratio of measured data/average DMSO control value times 100% to arrive at % activity.

MALDI TOF Method Intact Mw Analysis

Analyses were performed on a Shimadzu Biotech Axima TOF² (Shimadzu Instruments) matrix-assisted-laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometer. Proteins were analyzed in positive ion linear mode. For intact protein mass measurement the instrument was set with a mass range extending up to 75000 m/z using a pulsed extraction setting of 47000 and apomyoglobin as the standard to calibrate the instrument. A 3 ul aliquot of each sample was diluted with 7 ul of 0.1% TFA prior to micro C4 Zip Tip desalting and deposition directly onto the MALDI target using Sinapinic acid as the desorption matrix (10 mg/mL in 0.1% TFA:Acetonitrile 50:50).

Applicant's disclosure is described herein in preferred embodiments with reference to the Figures, in which like numbers represent the same or similar elements. Reference throughout this specification to “one embodiment,” “an embodiment,” or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases “in one embodiment,” “in an embodiment,” and similar language throughout this specification may, but do not necessarily, all refer to the same embodiment.

The described features, structures, or characteristics of Applicant's disclosure may be combined in any suitable manner in one or more embodiments. In the description, herein, numerous specific details are recited to provide a thorough understanding of embodiments of the invention. One skilled in the relevant art will recognize, however, that Applicant's composition and/or method may be practiced without one or more of the specific details, or with other methods, components, materials, and so forth. In other instances, well-known structures, materials, or operations are not shown or described in detail to avoid obscuring aspects of the disclosure.

In this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural reference, unless the context clearly dictates otherwise.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present disclosure, the preferred methods and materials are now described. Methods recited herein may be carried out in any order that is logically possible, in addition to a particular order disclosed.

INCORPORATION BY REFERENCE

References and citations to other documents, such as patents, patent applications, patent publications, journals, books, papers, web contents, have been made in this disclosure. All such documents are hereby incorporated herein by reference in their entirety for all purposes. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material explicitly set forth herein is only incorporated to the extent that no conflict arises between that incorporated material and the present disclosure material. In the event of a conflict, the conflict is to be resolved in favor of the present disclosure as the preferred disclosure.

EQUIVALENTS

The representative examples are intended to help illustrate the invention, and are not intended to, nor should they be construed to, limit the scope of the invention. Indeed, various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including the examples and the references to the scientific and patent literature included herein. The examples contain important additional information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof. 

1-36. (canceled)
 37. A method for treating, reducing, or preventing a disease or disorder, comprising administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula (I):

wherein, each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively; R_(E) is a group comprising an electrophilic warhead, or a pharmaceutically acceptable form thereof, or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.
 38. A method for treating, reducing, or preventing a disease or disorder, comprising administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula of (II):

wherein, each of R_(A) and R_(B) is independently H or a halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively; Z₁ and Z₂ is independently CH or N; R₁ is H or a halogen atom; and R₂ is a functional group that comprises an electrophilic group, or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.
 39. A method for treating, reducing, or preventing a disease or disorder, comprising administering to a subject in need thereof a pharmaceutical composition comprising a compound having the structural formula (III):

wherein, each of R_(A) and R_(B) is independently H or halogen, CN, CF₃, alkylamine, alkoxy and alky group, or R_(A) and R_(B) join together to form a 5-membered aromatic ring along with the two carbons (—C═C—) of the pyrimidine ring that R_(A) and R_(B) are bonded to respectively; Z₁ and Z₂ is independently CH or N; R₁ is H or a halogen atom; and R₂ is a functional group that comprises an electrophilic group, or a pharmaceutically acceptable form thereof, in an amount effective to treat, prevent, or reduce one or more cancers, or a related disease or disorder thereof, in a mammal, including a human, and a pharmaceutically acceptable excipient, carrier, or diluent.
 40. The method of claim 37, wherein the one or more cancers comprise a blood cancer or a hematologic malignance.
 41. The method of claim 40, wherein the one or more cancers are selected from B-acute lymphoblastic leukemias, B-acute lymphoblastic leukemias, chronic myelomonocytic leukemia, cute myelogenous leukemia, lymphoma, myelodysplasia syndrome, myeloproliferative neoplasms and myeloproliferative neoplasms.
 42. The method of claim 38, wherein the one or more cancers comprise a blood cancer or a hematologic malignance.
 43. The method of claim 42, wherein the one or more cancers are selected from B-acute lymphoblastic leukemias, B-acute lymphoblastic leukemias, chronic myelomonocytic leukemia, cute myelogenous leukemia, lymphoma, myelodysplasia syndrome, myeloproliferative neoplasms and myeloproliferative neoplasms.
 44. The method of claim 39, wherein the one or more cancers comprise a blood cancer or a hematologic malignance.
 45. The method of claim 44, wherein the one or more cancers are selected from B-acute lymphoblastic leukemias, B-acute lymphoblastic leukemias, chronic myelomonocytic leukemia, cute myelogenous leukemia, lymphoma, myelodysplasia syndrome, myeloproliferative neoplasms and myeloproliferative neoplasms. 